Canonical Allele Identifier: CA1582992061
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132053814T>A , CM000667.2:g.132053814T>A GRCh38
NC_000005.9:g.131389507T>A , CM000667.1:g.131389507T>A GRCh37
NC_000005.8:g.131417406T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948785.1:n.229-210A>T
XR_001742531.1:n.244-210A>T
XR_948785.2:n.252-210A>T