Canonical Allele Identifier: CA15652760

Gene: FAS

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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