Canonical Allele Identifier: CA421944446
Gene: FASLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.172634838T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665698T>C , CM000663.2:g.172665698T>C GRCh38
NC_000001.10:g.172634838T>C , CM000663.1:g.172634838T>C GRCh37
NC_000001.9:g.170901461T>C NCBI36
NG_007269.1:g.11654T>C , LRG_58:g.11654T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.528T>C MANE Select ENSP00000356694.2:p.Tyr176=
ENST00000340030.4:c.*98T>C ENSP00000344739.3:n.*98T>C
ENST00000367721.2:c.528T>C ENSP00000356694.2:p.Tyr176=
NM_000639.2:c.528T>C NP_000630.1:p.Tyr176=
NM_001302746.1:c.*98T>C NP_001289675.1:n.*98T>C
NM_000639.3:c.528T>C MANE Select NP_000630.1:p.Tyr176=
NM_001302746.2:c.*98T>C NP_001289675.1:n.*98T>C
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