Canonical Allele Identifier: CA535731948
Gene:

Linked Data

dbSNP Id: rs1361255969

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120551863G>A , CM000664.2:g.120551863G>A GRCh38
NC_000002.11:g.121309439G>A , CM000664.1:g.121309439G>A GRCh37
NC_000002.10:g.121025909G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923262.1:n.1487+25C>T
XR_001739680.2:n.1495+25C>T
XR_001739681.2:n.2128+25C>T
XR_001739682.1:n.1495+25C>T
XR_002959417.1:n.1495+25C>T