Canonical Allele Identifier: CA2104891868
Community Standard Title: NC_000013.11:g.80118676G=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.80118676G= , CM000675.2:g.80118676G= GRCh38
NC_000013.10:g.80692811G= , CM000675.1:g.80692811G= GRCh37
NC_000013.9:g.79590812G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_942116.2:n.379C=