Canonical Allele Identifier: CA1041463649
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203934704T>A , CM000664.2:g.203934704T>A GRCh38
NC_000002.11:g.204799427T>A , CM000664.1:g.204799427T>A GRCh37
NC_000002.10:g.204507672T>A NCBI36
NG_011586.1:g.2925T>A , LRG_65:g.2925T>A

Transcript Alleles

HGVS Amino-acid change
XR_427213.2:n.460+1404A>T
XR_001739861.1:n.1564A>T
XR_427213.3:n.474+1404A>T