Canonical Allele Identifier: CA1960019974
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484081C= , CM000673.2:g.27484081C= GRCh38
NC_000011.9:g.27505628C= , CM000673.1:g.27505628C= GRCh37
NC_000011.8:g.27462204C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.232C=