Canonical Allele Identifier: CA163625040
Gene:

Linked Data

dbSNP Id: rs372141626
gnomAD v2: 7-97017771-A-G
gnomAD v3: 7-97388459-A-G
gnomAD v4: 7-97388459-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388459A>G , CM000669.2:g.97388459A>G GRCh38
NC_000007.13:g.97017771A>G , CM000669.1:g.97017771A>G GRCh37
NC_000007.12:g.96855707A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59812T>C