Canonical Allele Identifier: CA32979641
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1951037
ClinVar RCV Id: RCV002681685
dbSNP Id: rs372784586
gnomAD v2: 1-172634832-G-A
gnomAD v4: 1-172665692-G-A
MyVariant Identifiers: chr1:g.172634832G>A (hg19) chr1:g.172665692G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665692G>A , CM000663.2:g.172665692G>A GRCh38
NC_000001.10:g.172634832G>A , CM000663.1:g.172634832G>A GRCh37
NC_000001.9:g.170901455G>A NCBI36
NG_007269.1:g.11648G>A , LRG_58:g.11648G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.522G>A MANE Select ENSP00000356694.2:p.Val174=
ENST00000340030.4:c.*92G>A ENSP00000344739.3:n.*92G>A
ENST00000367721.2:c.522G>A ENSP00000356694.2:p.Val174=
NM_000639.2:c.522G>A NP_000630.1:p.Val174=
NM_001302746.1:c.*92G>A NP_001289675.1:n.*92G>A
NM_000639.3:c.522G>A MANE Select NP_000630.1:p.Val174=
NM_001302746.2:c.*92G>A NP_001289675.1:n.*92G>A
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