Canonical Allele Identifier: CA2580584529
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172741860T>A , CM000663.2:g.172741860T>A GRCh38
NC_000001.10:g.172711000T>A , CM000663.1:g.172711000T>A GRCh37
NC_000001.9:g.170977623T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922289.1:n.27-33959T>A