Canonical Allele Identifier: CA1818149922
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999788C= , CM000670.2:g.126999788C= GRCh38
NC_000008.10:g.128012033C= , CM000670.1:g.128012033C= GRCh37
NC_000008.9:g.128081215C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6767C=