Canonical Allele Identifier: CA535731949
Gene:

Linked Data

dbSNP Id: rs1448354129

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120551865G>A , CM000664.2:g.120551865G>A GRCh38
NC_000002.11:g.121309441G>A , CM000664.1:g.121309441G>A GRCh37
NC_000002.10:g.121025911G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923262.1:n.1487+23C>T
XR_001739680.2:n.1495+23C>T
XR_001739681.2:n.2128+23C>T
XR_001739682.1:n.1495+23C>T
XR_002959417.1:n.1495+23C>T