Canonical Allele Identifier: CA343806033
Gene: FASLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.172634831T>A (hg19) chr1:g.172665691T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665691T>A , CM000663.2:g.172665691T>A GRCh38
NC_000001.10:g.172634831T>A , CM000663.1:g.172634831T>A GRCh37
NC_000001.9:g.170901454T>A NCBI36
NG_007269.1:g.11647T>A , LRG_58:g.11647T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.521T>A MANE Select ENSP00000356694.2:p.Val174Glu
ENST00000340030.4:c.*91T>A ENSP00000344739.3:n.*91T>A
ENST00000367721.2:c.521T>A ENSP00000356694.2:p.Val174Glu
NM_000639.2:c.521T>A NP_000630.1:p.Val174Glu
NM_001302746.1:c.*91T>A NP_001289675.1:n.*91T>A
NM_000639.3:c.521T>A MANE Select NP_000630.1:p.Val174Glu
NM_001302746.2:c.*91T>A NP_001289675.1:n.*91T>A
Search 100 bp 5'
Search 100 bp 3'