Canonical Allele Identifier: CA163625032
Gene:

Linked Data

dbSNP Id: rs541860457
gnomAD v2: 7-97017665-T-A
gnomAD v3: 7-97388353-T-A
gnomAD v4: 7-97388353-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388353T>A , CM000669.2:g.97388353T>A GRCh38
NC_000007.13:g.97017665T>A , CM000669.1:g.97017665T>A GRCh37
NC_000007.12:g.96855601T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745293.1:n.127-59706A>T