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AATTAACTAAAACAATTACATATAT[A/T]TTTTTTTTCAAATTTAGTCAGCTAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600003 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CACNB2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
CACNB2 - calcium voltage-gated channel auxiliary subunit beta 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000724.3 | Intron | NP_000715.2 | ||||
NM_001167945.1 | Intron | NP_001161417.1 | ||||
NM_201570.2 | Intron | NP_963864.1 | ||||
NM_201571.3 | Intron | NP_963865.2 | ||||
NM_201572.3 | Intron | NP_963866.2 | ||||
NM_201590.2 | Intron | NP_963884.2 | ||||
NM_201593.2 | Intron | NP_963887.2 | ||||
NM_201596.2 | Intron | NP_963890.2 | ||||
NM_201597.2 | Intron | NP_963891.1 | ||||
XM_005252588.3 | Intron | XP_005252645.1 | ||||
XM_005252591.3 | Intron | XP_005252648.1 | ||||
XM_006717502.3 | Intron | XP_006717565.1 | ||||
XM_011519659.2 | Intron | XP_011517961.1 | ||||
XM_011519660.2 | Intron | XP_011517962.1 | ||||
XM_017016625.1 | Intron | XP_016872114.1 |