Canonical Allele Identifier: CA343806154
Gene: FASLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.172634887T>C (hg19) chr1:g.172665747T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665747T>C , CM000663.2:g.172665747T>C GRCh38
NC_000001.10:g.172634887T>C , CM000663.1:g.172634887T>C GRCh37
NC_000001.9:g.170901510T>C NCBI36
NG_007269.1:g.11703T>C , LRG_58:g.11703T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.577T>C MANE Select ENSP00000356694.2:p.Ser193Pro
ENST00000340030.4:c.*147T>C ENSP00000344739.3:n.*147T>C
ENST00000367721.2:c.577T>C ENSP00000356694.2:p.Ser193Pro
NM_000639.2:c.577T>C NP_000630.1:p.Ser193Pro
NM_001302746.1:c.*147T>C NP_001289675.1:n.*147T>C
NM_000639.3:c.577T>C MANE Select NP_000630.1:p.Ser193Pro
NM_001302746.2:c.*147T>C NP_001289675.1:n.*147T>C
Search 100 bp 5'
Search 100 bp 3'