Canonical Allele Identifier: CA2504937660
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.25831413C>T , CM000669.2:g.25831413C>T GRCh38
NC_000007.13:g.25871033C>T , CM000669.1:g.25871033C>T GRCh37
NC_000007.12:g.25837558C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_108752.3:n.494G>A
XR_927108.1:n.468G>A
XR_927109.1:n.550G>A
XR_927110.1:n.454G>A
XR_108752.4:n.508G>A
XR_927110.2:n.633G>A