Canonical Allele Identifier: CA1818149963
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999810C= , CM000670.2:g.126999810C= GRCh38
NC_000008.10:g.128012055C= , CM000670.1:g.128012055C= GRCh37
NC_000008.9:g.128081237C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6745C=