Canonical Allele Identifier: CA1033291358
Gene:

Linked Data

dbSNP Id: rs1672683671
gnomAD v3: 2-88016318-T-A
gnomAD v4: 2-88016318-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016318T>A , CM000664.2:g.88016318T>A GRCh38
NC_000002.11:g.88315837T>A , CM000664.1:g.88315837T>A GRCh37
NC_000002.10:g.88096952T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.663T>A
XR_940336.3:n.663T>A