Canonical Allele Identifier: CA1283591736
Gene:

Linked Data

dbSNP Id: rs1327337568

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120551858C>A , CM000664.2:g.120551858C>A GRCh38
NC_000002.11:g.121309434C>A , CM000664.1:g.121309434C>A GRCh37
NC_000002.10:g.121025904C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923262.1:n.1487+30G>T
XR_001739680.2:n.1495+30G>T
XR_001739681.2:n.2128+30G>T
XR_001739682.1:n.1495+30G>T
XR_002959417.1:n.1495+30G>T