Canonical Allele Identifier: CA1985859959
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.80851723C= , CM000673.2:g.80851723C= GRCh38
NC_000011.9:g.80562766C= , CM000673.1:g.80562766C= GRCh37
NC_000011.8:g.80240414C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247272.2:n.124+60568G=