Canonical Allele Identifier: CA1552561729
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.66487875C= , CM000667.2:g.66487875C= GRCh38
NC_000005.9:g.65783703C= , CM000667.1:g.65783703C= GRCh37
NC_000005.8:g.65819459C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948381.1:n.649-48961C=