Canonical Allele Identifier: CA2581187892
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92314657T>A , CM000676.2:g.92314657T>A GRCh38
NC_000014.8:g.92781001T>A , CM000676.1:g.92781001T>A GRCh37
NC_000014.7:g.91850754T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_944153.1:n.132-589T>A