Canonical Allele Identifier: CA341738
Gene: FASLG HGNC NCBI
MyVariant.info:
GRCh38 chr1:g.172665636A>G
GRCh37 chr1:g.172634776A>G
Revel Score:
ENST00000367721 (MANE Select) 0.284
gnomAD v2:
1:172634776 A / G
gnomAD v3:
1:172665636 A / G
gnomAD v4:
chr1-172665636-A-G
Joint Max Group AF 0.00012664 (NFE)
Genomes Max Group AF 0.00007907 (NFE)
Exomes Max Group AF 0.00012622 (NFE)
ClinVar RCV:
RCV000020369
RCV002476995
ClinVar Variation:
21212
dbSNP:
80358238
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665636A>G , CM000663.2:g.172665636A>G GRCh38
NC_000001.10:g.172634776A>G , CM000663.1:g.172634776A>G GRCh37
NC_000001.9:g.170901399A>G NCBI36
NG_007269.1:g.11592A>G , LRG_58:g.11592A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.466A>G MANE Select ENSP00000356694.2:p.Arg156Gly
ENST00000340030.4:c.*36A>G ENSP00000344739.3:n.*36A>G
ENST00000367721.2:c.466A>G ENSP00000356694.2:p.Arg156Gly
NM_000639.2:c.466A>G NP_000630.1:p.Arg156Gly
NM_001302746.1:c.*36A>G NP_001289675.1:n.*36A>G
NM_000639.3:c.466A>G MANE Select NP_000630.1:p.Arg156Gly
NM_001302746.2:c.*36A>G NP_001289675.1:n.*36A>G
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