Canonical Allele Identifier: CA32979644
Gene: FASLG HGNC NCBI

Linked Data

dbSNP Id: rs900252191
gnomAD v2: 1-172634861-A-G
gnomAD v3: 1-172665721-A-G
gnomAD v4: 1-172665721-A-G
MyVariant Identifiers: chr1:g.172634861A>G (hg19) chr1:g.172665721A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665721A>G , CM000663.2:g.172665721A>G GRCh38
NC_000001.10:g.172634861A>G , CM000663.1:g.172634861A>G GRCh37
NC_000001.9:g.170901484A>G NCBI36
NG_007269.1:g.11677A>G , LRG_58:g.11677A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.551A>G MANE Select ENSP00000356694.2:p.Asn184Ser
ENST00000340030.4:c.*121A>G ENSP00000344739.3:n.*121A>G
ENST00000367721.2:c.551A>G ENSP00000356694.2:p.Asn184Ser
NM_000639.2:c.551A>G NP_000630.1:p.Asn184Ser
NM_001302746.1:c.*121A>G NP_001289675.1:n.*121A>G
NM_000639.3:c.551A>G MANE Select NP_000630.1:p.Asn184Ser
NM_001302746.2:c.*121A>G NP_001289675.1:n.*121A>G
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