Canonical Allele Identifier: CA1596629099
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162656531C= , CM000667.2:g.162656531C= GRCh38
NC_000005.9:g.162083537C= , CM000667.1:g.162083537C= GRCh37
NC_000005.8:g.162016115C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742958.1:n.418+3571G=