Canonical Allele Identifier: CA1596629029
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.162656458G= , CM000667.2:g.162656458G= GRCh38
NC_000005.9:g.162083464G= , CM000667.1:g.162083464G= GRCh37
NC_000005.8:g.162016042G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742958.1:n.418+3644C=