Canonical Allele Identifier: CA1960019970
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484075T= , CM000673.2:g.27484075T= GRCh38
NC_000011.9:g.27505622T= , CM000673.1:g.27505622T= GRCh37
NC_000011.8:g.27462198T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.226T=