Canonical Allele Identifier: CA891270325

Gene: TNFSF4

Linked Data

• dbSNP Id: rs1384477238
• MyVariant Identifiers: chr1:g.173156393A>G (hg19) ; chr1:g.173187254A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173187254A>G , CM000663.2:g.173187254A>G	GRCh38
NC_000001.10:g.173156393A>G , CM000663.1:g.173156393A>G	GRCh37
NC_000001.9:g.171423016A>G	NCBI36
NG_011477.1:g.25079T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.203-389T>C MANE Select	ENSP00000281834.3:n.203-389T>C
ENST00000281834.3:c.203-389T>C	ENSP00000281834.3:n.203-389T>C
ENST00000367718.5:c.53-389T>C	ENSP00000356691.1:n.53-389T>C
NM_001297562.1:c.53-389T>C	NP_001284491.1:n.53-389T>C
NM_003326.4:c.203-389T>C	NP_003317.1:n.203-389T>C
XM_011509964.1:c.275-389T>C	XP_011508266.1:n.275-389T>C
XM_011509964.2:c.491-389T>C	XP_011508266.2:n.491-389T>C
XM_017002228.1:c.299-389T>C	XP_016857717.1:n.299-389T>C
XM_017002229.1:c.236-389T>C	XP_016857718.1:n.236-389T>C
XM_017002230.1:c.230-389T>C	XP_016857719.1:n.230-389T>C
NM_003326.5:c.203-389T>C MANE Select	NP_003317.1:n.203-389T>C
NM_001297562.2:c.53-389T>C	NP_001284491.1:n.53-389T>C