Canonical Allele Identifier: CA343805998
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 650472
ClinVar RCV Id: RCV000805632
dbSNP Id: rs1291566237
gnomAD v3: 1-172665673-T-A
gnomAD v4: 1-172665673-T-A
MyVariant Identifiers: chr1:g.172634813T>A (hg19) chr1:g.172665673T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665673T>A , CM000663.2:g.172665673T>A GRCh38
NC_000001.10:g.172634813T>A , CM000663.1:g.172634813T>A GRCh37
NC_000001.9:g.170901436T>A NCBI36
NG_007269.1:g.11629T>A , LRG_58:g.11629T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.503T>A MANE Select ENSP00000356694.2:p.Ile168Asn
ENST00000340030.4:c.*73T>A ENSP00000344739.3:n.*73T>A
ENST00000367721.2:c.503T>A ENSP00000356694.2:p.Ile168Asn
NM_000639.2:c.503T>A NP_000630.1:p.Ile168Asn
NM_001302746.1:c.*73T>A NP_001289675.1:n.*73T>A
NM_000639.3:c.503T>A MANE Select NP_000630.1:p.Ile168Asn
NM_001302746.2:c.*73T>A NP_001289675.1:n.*73T>A
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