Canonical Allele Identifier: CA2355978692
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661630T= , CM000682.2:g.23661630T= GRCh38
NC_000020.10:g.23642267T= , CM000682.1:g.23642267T= GRCh37
NC_000020.9:g.23590267T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.260T=