Canonical Allele Identifier: CA1960019991
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484124G= , CM000673.2:g.27484124G= GRCh38
NC_000011.9:g.27505671G= , CM000673.1:g.27505671G= GRCh37
NC_000011.8:g.27462247G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.275G=