Canonical Allele Identifier: CA2355978697
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661637C= , CM000682.2:g.23661637C= GRCh38
NC_000020.10:g.23642274C= , CM000682.1:g.23642274C= GRCh37
NC_000020.9:g.23590274C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.267C=