Canonical Allele Identifier: CA1960019978
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484086T= , CM000673.2:g.27484086T= GRCh38
NC_000011.9:g.27505633T= , CM000673.1:g.27505633T= GRCh37
NC_000011.8:g.27462209T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.237T=