Canonical Allele Identifier: CA1926643638
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89023563C= , CM000672.2:g.89023563C= GRCh38
NC_000010.10:g.90783320C= , CM000672.1:g.90783320C= GRCh37
NC_000010.9:g.90773300C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000690268.1:c.*9113C= ENSP00000509810.1:n.*9113C=