Canonical Allele Identifier: CA2700309410
Gene:

Linked Data

dbSNP Id: rs2104659848

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884110G>T , CM000664.2:g.122884110G>T GRCh38
NC_000002.11:g.123641686G>T , CM000664.1:g.123641686G>T GRCh37
NC_000002.10:g.123358156G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-832G>T
XR_001739692.1:n.1451-832G>T
XR_923292.2:n.1358-832G>T