Canonical Allele Identifier: CA1960019992
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484126T= , CM000673.2:g.27484126T= GRCh38
NC_000011.9:g.27505673T= , CM000673.1:g.27505673T= GRCh37
NC_000011.8:g.27462249T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.277T=