Canonical Allele Identifier: CA11075013
Gene:

Linked Data

dbSNP Id: rs12714207
gnomAD v2: 2-88315793-C-T
gnomAD v3: 2-88016274-C-T
gnomAD v4: 2-88016274-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016274C>T , CM000664.2:g.88016274C>T GRCh38
NC_000002.11:g.88315793C>T , CM000664.1:g.88315793C>T GRCh37
NC_000002.10:g.88096908C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.619C>T
XR_940336.3:n.619C>T