Canonical Allele Identifier: CA2355978700
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661642C= , CM000682.2:g.23661642C= GRCh38
NC_000020.10:g.23642279C= , CM000682.1:g.23642279C= GRCh37
NC_000020.9:g.23590279C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001754712.1:n.272C=