Canonical Allele Identifier: CA8350831

Gene: TNFSF12 TNFSF12-TNFSF13

Linked Data

• ClinVar Variation Id: 225690
• ClinVar RCV Id: RCV000211031 ; RCV001358814
• dbSNP Id: rs540997935
• ExAC: 17:7460154 C / T
• gnomAD v2: 17-7460154-C-T
• gnomAD v3: 17-7556837-C-T
• gnomAD v4: 17-7556837-C-T
• MyVariant Identifiers: chr17:g.7460154C>T (hg19) ; chr17:g.7556837C>T (hg38)
• PubMed: PMID:23493554

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7556837C>T , CM000679.2:g.7556837C>T	GRCh38
NC_000017.10:g.7460154C>T , CM000679.1:g.7460154C>T	GRCh37
NC_000017.9:g.7400878C>T	NCBI36
NG_029949.1:g.3546C>T
NG_052944.1:g.12780C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462619.6:n.550C>T (TNFSF12)
ENST00000462811.2:n.271C>T (TNFSF12)
ENST00000700014.1:c.*143C>T (TNFSF12)	ENSP00000514755.1:n.*143C>T
ENST00000700015.1:c.436C>T (TNFSF12)	ENSP00000514756.1:p.Arg146Cys
ENST00000700047.1:n.435C>T (TNFSF12)
ENST00000700048.1:n.677C>T (TNFSF12)
ENST00000700049.1:n.429C>T (TNFSF12)
ENST00000700050.1:n.680C>T (TNFSF12)
ENST00000700052.1:c.374-262C>T (TNFSF12)	ENSP00000514764.1:n.374-262C>T
ENST00000700053.1:c.430C>T (TNFSF12)	ENSP00000514765.1:p.Arg144Cys
ENST00000700054.1:c.*143C>T (TNFSF12)	ENSP00000514766.1:n.*143C>T
ENST00000700056.1:c.*267C>T (TNFSF12)	ENSP00000514767.1:n.*267C>T
ENST00000700057.1:n.521C>T (TNFSF12)
ENST00000700058.1:n.535C>T (TNFSF12)
ENST00000700059.1:n.802C>T (TNFSF12)
ENST00000293825.11:c.433C>T (TNFSF12) MANE Select	ENSP00000293825.6:p.Arg145Cys
ENST00000293825.10:c.433C>T (TNFSF12)	ENSP00000293825.6:p.Arg145Cys
ENST00000293826.4:c.433C>T (TNFSF12-TNFSF13)	ENSP00000293826.4:p.Arg145Cys
ENST00000322272.11:c.*267C>T (TNFSF12)	ENSP00000314636.7:n.*267C>T
ENST00000462619.5:n.323C>T (TNFSF12)
ENST00000462811.1:n.264C>T (TNFSF12)
NM_003809.2:c.433C>T (TNFSF12)	NP_003800.1:p.Arg145Cys
NM_172089.3:c.433C>T (TNFSF12-TNFSF13)	NP_742086.1:p.Arg145Cys
NR_037146.1:n.768C>T (TNFSF12)
NM_003809.3:c.433C>T (TNFSF12) MANE Select	NP_003800.1:p.Arg145Cys
NM_172089.4:c.433C>T (TNFSF12-TNFSF13)	NP_742086.1:p.Arg145Cys
NR_037146.2:n.768C>T (TNFSF12)