Canonical Allele Identifier: CA533736768
Gene:

Linked Data

dbSNP Id: rs1218850731
gnomAD v2: 2-74939089-C-T
gnomAD v3: 2-74711962-C-T
gnomAD v4: 2-74711962-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74711962C>T , CM000664.2:g.74711962C>T GRCh38
NC_000002.11:g.74939089C>T , CM000664.1:g.74939089C>T GRCh37
NC_000002.10:g.74792597C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427047.4:n.275C>T