Canonical Allele Identifier: CA47693354
Gene:

Linked Data

dbSNP Id: rs1012586144
gnomAD v2: 2-52949596-T-C
gnomAD v3: 2-52722458-T-C
gnomAD v4: 2-52722458-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722458T>C , CM000664.2:g.52722458T>C GRCh38
NC_000002.11:g.52949596T>C , CM000664.1:g.52949596T>C GRCh37
NC_000002.10:g.52803100T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.799A>G