Canonical Allele Identifier: CA1698033033
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.31115733T>A , CM000669.2:g.31115733T>A GRCh38
NC_000007.13:g.31155347T>A , CM000669.1:g.31155347T>A GRCh37
NC_000007.12:g.31121872T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002956556.1:n.8284A>T