Canonical Allele Identifier: CA1322177712
Gene:

Linked Data

dbSNP Id: rs1689615683

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203934597C>A , CM000664.2:g.203934597C>A GRCh38
NC_000002.11:g.204799320C>A , CM000664.1:g.204799320C>A GRCh37
NC_000002.10:g.204507565C>A NCBI36
NG_011586.1:g.2818C>A , LRG_65:g.2818C>A

Transcript Alleles

HGVS Amino-acid change
XR_427213.2:n.460+1511G>T
XR_001739861.1:n.1671G>T
XR_427213.3:n.474+1511G>T