Canonical Allele Identifier: CA343806190
Gene: FASLG HGNC NCBI

Linked Data

gnomAD v4: 1-172665763-G-A
MyVariant Identifiers: chr1:g.172634903G>A (hg19) chr1:g.172665763G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665763G>A , CM000663.2:g.172665763G>A GRCh38
NC_000001.10:g.172634903G>A , CM000663.1:g.172634903G>A GRCh37
NC_000001.9:g.170901526G>A NCBI36
NG_007269.1:g.11719G>A , LRG_58:g.11719G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.593G>A MANE Select ENSP00000356694.2:p.Arg198Gln
ENST00000340030.4:c.*163G>A ENSP00000344739.3:n.*163G>A
ENST00000367721.2:c.593G>A ENSP00000356694.2:p.Arg198Gln
NM_000639.2:c.593G>A NP_000630.1:p.Arg198Gln
NM_001302746.1:c.*163G>A NP_001289675.1:n.*163G>A
NM_000639.3:c.593G>A MANE Select NP_000630.1:p.Arg198Gln
NM_001302746.2:c.*163G>A NP_001289675.1:n.*163G>A
Search 100 bp 5'
Search 100 bp 3'