Canonical Allele Identifier: CA32979629
Gene: FASLG HGNC NCBI

Linked Data

dbSNP Id: rs565446606
gnomAD v2: 1-172634689-T-G
gnomAD v3: 1-172665549-T-G
gnomAD v4: 1-172665549-T-G
MyVariant Identifiers: chr1:g.172634689T>G (hg19) chr1:g.172665549T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665549T>G , CM000663.2:g.172665549T>G GRCh38
NC_000001.10:g.172634689T>G , CM000663.1:g.172634689T>G GRCh37
NC_000001.9:g.170901312T>G NCBI36
NG_007269.1:g.11505T>G , LRG_58:g.11505T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.452-73T>G MANE Select ENSP00000356694.2:n.452-73T>G
ENST00000340030.4:c.*22-73T>G ENSP00000344739.3:n.*22-73T>G
ENST00000367721.2:c.452-73T>G ENSP00000356694.2:n.452-73T>G
NM_000639.2:c.452-73T>G NP_000630.1:n.452-73T>G
NM_001302746.1:c.*22-73T>G NP_001289675.1:n.*22-73T>G
NM_000639.3:c.452-73T>G MANE Select NP_000630.1:n.452-73T>G
NM_001302746.2:c.*22-73T>G NP_001289675.1:n.*22-73T>G
Search 100 bp 5'
Search 100 bp 3'