Canonical Allele Identifier: CA343806047
Gene: FASLG HGNC NCBI

Linked Data

dbSNP Id: rs1347125362
gnomAD v2: 1-172634837-A-G
gnomAD v4: 1-172665697-A-G
MyVariant Identifiers: chr1:g.172634837A>G (hg19) chr1:g.172665697A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665697A>G , CM000663.2:g.172665697A>G GRCh38
NC_000001.10:g.172634837A>G , CM000663.1:g.172634837A>G GRCh37
NC_000001.9:g.170901460A>G NCBI36
NG_007269.1:g.11653A>G , LRG_58:g.11653A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.527A>G MANE Select ENSP00000356694.2:p.Tyr176Cys
ENST00000340030.4:c.*97A>G ENSP00000344739.3:n.*97A>G
ENST00000367721.2:c.527A>G ENSP00000356694.2:p.Tyr176Cys
NM_000639.2:c.527A>G NP_000630.1:p.Tyr176Cys
NM_001302746.1:c.*97A>G NP_001289675.1:n.*97A>G
NM_000639.3:c.527A>G MANE Select NP_000630.1:p.Tyr176Cys
NM_001302746.2:c.*97A>G NP_001289675.1:n.*97A>G
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