Canonical Allele Identifier: CA15613972
Gene:
MyVariant.info:
GRCh38 chr9:g.1456797C>T
GRCh37 chr9:g.1456797C>T
gnomAD v2:
9:1456797 C / T
gnomAD v3:
9:1456797 C / T
gnomAD v4:
chr9-1456797-C-T
Joint Max Group AF 0.50089649 (MID)
Genomes Max Group AF 0.41954281 (NFE)
dbSNP:
1412259
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.1456797C>T , CM000671.2:g.1456797C>T GRCh38
NC_000009.11:g.1456797C>T , CM000671.1:g.1456797C>T GRCh37
NC_000009.10:g.1446797C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929414.1:n.335-7346C>T
XR_929415.1:n.335-7346C>T
XR_929417.1:n.335-7346C>T
XR_002956872.1:n.338-7346C>T
XR_929415.2:n.338-7346C>T
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