Canonical Allele Identifier: CA1247594
Gene: FASLG HGNC NCBI

Linked Data

dbSNP Id: rs541085313
ExAC: 1:172634937 C / T
gnomAD v2: 1-172634937-C-T
gnomAD v3: 1-172665797-C-T
gnomAD v4: 1-172665797-C-T
MyVariant Identifiers: chr1:g.172634937C>T (hg19) chr1:g.172665797C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665797C>T , CM000663.2:g.172665797C>T GRCh38
NC_000001.10:g.172634937C>T , CM000663.1:g.172634937C>T GRCh37
NC_000001.9:g.170901560C>T NCBI36
NG_007269.1:g.11753C>T , LRG_58:g.11753C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.627C>T MANE Select ENSP00000356694.2:p.His209=
ENST00000340030.4:c.*197C>T ENSP00000344739.3:n.*197C>T
ENST00000367721.2:c.627C>T ENSP00000356694.2:p.His209=
NM_000639.2:c.627C>T NP_000630.1:p.His209=
NM_001302746.1:c.*197C>T NP_001289675.1:n.*197C>T
NM_000639.3:c.627C>T MANE Select NP_000630.1:p.His209=
NM_001302746.2:c.*197C>T NP_001289675.1:n.*197C>T
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