Canonical Allele Identifier: CA539151231
Gene:

Linked Data

dbSNP Id: rs1314543702

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203934706G>A , CM000664.2:g.203934706G>A GRCh38
NC_000002.11:g.204799429G>A , CM000664.1:g.204799429G>A GRCh37
NC_000002.10:g.204507674G>A NCBI36
NG_011586.1:g.2927G>A , LRG_65:g.2927G>A

Transcript Alleles

HGVS Amino-acid change
XR_427213.2:n.460+1402C>T
XR_001739861.1:n.1562C>T
XR_427213.3:n.474+1402C>T