Canonical Allele Identifier: CA891226254
Gene: FASLG HGNC NCBI

Linked Data

dbSNP Id: rs767244050
gnomAD v3: 1-172664259-T-C
gnomAD v4: 1-172664259-T-C
MyVariant Identifiers: chr1:g.172633399T>C (hg19) chr1:g.172664259T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172664259T>C , CM000663.2:g.172664259T>C GRCh38
NC_000001.10:g.172633399T>C , CM000663.1:g.172633399T>C GRCh37
NC_000001.9:g.170900022T>C NCBI36
NG_007269.1:g.10215T>C , LRG_58:g.10215T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.395-75T>C MANE Select ENSP00000356694.2:n.395-75T>C
ENST00000340030.4:c.349-75T>C ENSP00000344739.3:n.349-75T>C
ENST00000367721.2:c.395-75T>C ENSP00000356694.2:n.395-75T>C
NM_000639.2:c.395-75T>C NP_000630.1:n.395-75T>C
NM_001302746.1:c.349-75T>C NP_001289675.1:n.349-75T>C
NM_000639.3:c.395-75T>C MANE Select NP_000630.1:n.395-75T>C
NM_001302746.2:c.349-75T>C NP_001289675.1:n.349-75T>C
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