Canonical Allele Identifier: CA1796167917
Community Standard Title: NC_000008.11:g.78663569T=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.78663569T= , CM000670.2:g.78663569T= GRCh38
NC_000008.10:g.79575804T= , CM000670.1:g.79575804T= GRCh37
NC_000008.9:g.79738359T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001745972.1:n.963+1436A=
XR_929074.1:n.975+1436A=