Canonical Allele Identifier: CA1174420503
Gene:

Linked Data

dbSNP Id: rs10458561

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.70455490G>T , CM000663.2:g.70455490G>T GRCh38
NC_000001.10:g.70921173G>T , CM000663.1:g.70921173G>T GRCh37
NC_000001.9:g.70693761G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_947499.1:n.400-2641G>T
XR_947499.2:n.411-2641G>T