Canonical Allele Identifier: CA421944417
Gene: FASLG HGNC NCBI

Linked Data

dbSNP Id: rs1659242186
gnomAD v3: 1-172665662-C-T
gnomAD v4: 1-172665662-C-T
MyVariant Identifiers: chr1:g.172634802C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665662C>T , CM000663.2:g.172665662C>T GRCh38
NC_000001.10:g.172634802C>T , CM000663.1:g.172634802C>T GRCh37
NC_000001.9:g.170901425C>T NCBI36
NG_007269.1:g.11618C>T , LRG_58:g.11618C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.492C>T MANE Select ENSP00000356694.2:p.Asp164=
ENST00000340030.4:c.*62C>T ENSP00000344739.3:n.*62C>T
ENST00000367721.2:c.492C>T ENSP00000356694.2:p.Asp164=
NM_000639.2:c.492C>T NP_000630.1:p.Asp164=
NM_001302746.1:c.*62C>T NP_001289675.1:n.*62C>T
NM_000639.3:c.492C>T MANE Select NP_000630.1:p.Asp164=
NM_001302746.2:c.*62C>T NP_001289675.1:n.*62C>T
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