Canonical Allele Identifier: CA1284674227
Gene:

Linked Data

dbSNP Id: rs1680375171

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884085G>A , CM000664.2:g.122884085G>A GRCh38
NC_000002.11:g.123641661G>A , CM000664.1:g.123641661G>A GRCh37
NC_000002.10:g.123358131G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-857G>A
XR_001739692.1:n.1451-857G>A
XR_923292.2:n.1358-857G>A