Canonical Allele Identifier: CA11255757
Gene:

Linked Data

dbSNP Id: rs17367118

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122884035G>A , CM000664.2:g.122884035G>A GRCh38
NC_000002.11:g.123641611G>A , CM000664.1:g.123641611G>A GRCh37
NC_000002.10:g.123358081G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923292.1:n.1125-907G>A
XR_001739692.1:n.1451-907G>A
XR_923292.2:n.1358-907G>A