Canonical Allele Identifier: CA2355978789
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23661835T= , CM000682.2:g.23661835T= GRCh38
NC_000020.10:g.23642472T= , CM000682.1:g.23642472T= GRCh37
NC_000020.9:g.23590472T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001754712.1:n.280+185T=