Canonical Allele Identifier: CA343806098
Gene: FASLG HGNC NCBI

Linked Data

gnomAD v4: 1-172665721-A-C
MyVariant Identifiers: chr1:g.172634861A>C (hg19) chr1:g.172665721A>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.551A>C MANE Select ENSP00000356694.2:p.Asn184Thr
ENST00000340030.4:c.*121A>C ENSP00000344739.3:n.*121A>C
ENST00000367721.2:c.551A>C ENSP00000356694.2:p.Asn184Thr
NM_000639.2:c.551A>C NP_000630.1:p.Asn184Thr
NM_001302746.1:c.*121A>C NP_001289675.1:n.*121A>C
NM_000639.3:c.551A>C MANE Select NP_000630.1:p.Asn184Thr
NM_001302746.2:c.*121A>C NP_001289675.1:n.*121A>C
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