Canonical Allele Identifier: CA51878291
Gene:

Linked Data

dbSNP Id: rs369516133
gnomAD v2: 2-88315699-C-A
gnomAD v3: 2-88016180-C-A
gnomAD v4: 2-88016180-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016180C>A , CM000664.2:g.88016180C>A GRCh38
NC_000002.11:g.88315699C>A , CM000664.1:g.88315699C>A GRCh37
NC_000002.10:g.88096814C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940335.3:n.525C>A
XR_940336.3:n.525C>A