Canonical Allele Identifier: CA343806136
Gene: FASLG HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.172634879T>C (hg19) chr1:g.172665739T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665739T>C , CM000663.2:g.172665739T>C GRCh38
NC_000001.10:g.172634879T>C , CM000663.1:g.172634879T>C GRCh37
NC_000001.9:g.170901502T>C NCBI36
NG_007269.1:g.11695T>C , LRG_58:g.11695T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.569T>C MANE Select ENSP00000356694.2:p.Phe190Ser
ENST00000340030.4:c.*139T>C ENSP00000344739.3:n.*139T>C
ENST00000367721.2:c.569T>C ENSP00000356694.2:p.Phe190Ser
NM_000639.2:c.569T>C NP_000630.1:p.Phe190Ser
NM_001302746.1:c.*139T>C NP_001289675.1:n.*139T>C
NM_000639.3:c.569T>C MANE Select NP_000630.1:p.Phe190Ser
NM_001302746.2:c.*139T>C NP_001289675.1:n.*139T>C
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