Canonical Allele Identifier: CA1247587
Gene: FASLG HGNC NCBI

Linked Data

dbSNP Id: rs747293631
ExAC: 1:172634855 T / G
gnomAD v2: 1-172634855-T-G
gnomAD v4: 1-172665715-T-G
MyVariant Identifiers: chr1:g.172634855T>G (hg19) chr1:g.172665715T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665715T>G , CM000663.2:g.172665715T>G GRCh38
NC_000001.10:g.172634855T>G , CM000663.1:g.172634855T>G GRCh37
NC_000001.9:g.170901478T>G NCBI36
NG_007269.1:g.11671T>G , LRG_58:g.11671T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.545T>G MANE Select ENSP00000356694.2:p.Val182Gly
ENST00000340030.4:c.*115T>G ENSP00000344739.3:n.*115T>G
ENST00000367721.2:c.545T>G ENSP00000356694.2:p.Val182Gly
NM_000639.2:c.545T>G NP_000630.1:p.Val182Gly
NM_001302746.1:c.*115T>G NP_001289675.1:n.*115T>G
NM_000639.3:c.545T>G MANE Select NP_000630.1:p.Val182Gly
NM_001302746.2:c.*115T>G NP_001289675.1:n.*115T>G
Search 100 bp 5'
Search 100 bp 3'