Canonical Allele Identifier: CA1620959069
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.35569629T>A , CM000668.2:g.35569629T>A GRCh38
NC_000006.11:g.35537406T>A , CM000668.1:g.35537406T>A GRCh37
NC_000006.10:g.35645384T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_242006.2:n.433-23401T>A
XR_242006.3:n.462-23401T>A