Canonical Allele Identifier: CA126570
Gene: FAS HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 16501
ClinVar RCV Id: RCV000017965
dbSNP Id: rs121913077

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014259C>T , CM000672.2:g.89014259C>T GRCh38
NC_000010.9:g.90763996C>T NCBI36
NC_000010.10:g.90774016C>T , CM000672.1:g.90774016C>T GRCh37
NG_009089.2:g.28729C>T , LRG_134:g.28729C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000352159.8:c.*134C>T ENSP00000345601.4:p.=
ENST00000355279.2:n.792C>T ENSP00000347426.2:p.=
ENST00000355740.6:c.817C>T ENSP00000347979.2:p.Gln273Ter
ENST00000357339.6:c.754C>T ENSP00000349896.2:p.Gln252Ter
ENST00000479522.5:c.*246C>T ENSP00000424113.1:p.=
ENST00000484444.5:c.*258C>T ENSP00000420975.1:p.=
ENST00000488877.5:c.*258C>T ENSP00000425159.1:p.=
ENST00000492756.5:n.645C>T ENSP00000422453.1:p.=
ENST00000494410.5:c.*175C>T ENSP00000423755.1:p.=
ENST00000612663.4:c.*164C>T ENSP00000477997.2:p.=
NM_000043.4:c.817C>T , LRG_134t1:c.817C>T NP_000034.1:p.Gln273Ter
NM_152871.2:c.754C>T NP_690610.1:p.Gln252Ter
NM_152872.2:c.*129C>T NP_690611.1:p.=
NR_028033.2:n.991C>T
NR_028034.2:n.853C>T
NR_028035.2:n.916C>T
NR_028036.2:n.1054C>T
XM_006717819.2:c.898C>T XP_006717882.1:p.Gln300Ter
XM_011539764.1:c.979C>T XP_011538066.1:p.Gln327Ter
XM_011539765.1:c.916C>T XP_011538067.1:p.Gln306Ter
XM_011539766.1:c.898C>T XP_011538068.1:p.Gln300Ter
XM_011539767.1:c.862C>T XP_011538069.1:p.Gln288Ter
XR_945732.1:n.885C>T
XR_945733.1:n.822C>T