Canonical Allele Identifier: CA1284673996
Gene:

Linked Data

dbSNP Id: rs1680370785

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883813G>A , CM000664.2:g.122883813G>A GRCh38
NC_000002.11:g.123641389G>A , CM000664.1:g.123641389G>A GRCh37
NC_000002.10:g.123357859G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-1129G>A
XR_001739692.1:n.1451-1129G>A
XR_923292.2:n.1358-1129G>A