Canonical Allele Identifier: CA421944594
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1567771
ClinVar RCV Id: RCV002210207
dbSNP Id: rs2101810683
MyVariant Identifiers: chr1:g.172634976G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665836G>A , CM000663.2:g.172665836G>A GRCh38
NC_000001.10:g.172634976G>A , CM000663.1:g.172634976G>A GRCh37
NC_000001.9:g.170901599G>A NCBI36
NG_007269.1:g.11792G>A , LRG_58:g.11792G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.666G>A MANE Select ENSP00000356694.2:p.Leu222=
ENST00000340030.4:c.*236G>A ENSP00000344739.3:n.*236G>A
ENST00000367721.2:c.666G>A ENSP00000356694.2:p.Leu222=
NM_000639.2:c.666G>A NP_000630.1:p.Leu222=
NM_001302746.1:c.*236G>A NP_001289675.1:n.*236G>A
NM_000639.3:c.666G>A MANE Select NP_000630.1:p.Leu222=
NM_001302746.2:c.*236G>A NP_001289675.1:n.*236G>A
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