Canonical Allele Identifier: CA32979642
Gene: FASLG HGNC NCBI

Linked Data

dbSNP Id: rs944346006
gnomAD v2: 1-172634850-C-G
gnomAD v3: 1-172665710-C-G
gnomAD v4: 1-172665710-C-G
MyVariant Identifiers: chr1:g.172634850C>G (hg19) chr1:g.172665710C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665710C>G , CM000663.2:g.172665710C>G GRCh38
NC_000001.10:g.172634850C>G , CM000663.1:g.172634850C>G GRCh37
NC_000001.9:g.170901473C>G NCBI36
NG_007269.1:g.11666C>G , LRG_58:g.11666C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.540C>G MANE Select ENSP00000356694.2:p.Gly180=
ENST00000340030.4:c.*110C>G ENSP00000344739.3:n.*110C>G
ENST00000367721.2:c.540C>G ENSP00000356694.2:p.Gly180=
NM_000639.2:c.540C>G NP_000630.1:p.Gly180=
NM_001302746.1:c.*110C>G NP_001289675.1:n.*110C>G
NM_000639.3:c.540C>G MANE Select NP_000630.1:p.Gly180=
NM_001302746.2:c.*110C>G NP_001289675.1:n.*110C>G
Search 100 bp 5'
Search 100 bp 3'