Canonical Allele Identifier: CA891270385

Gene: TNFSF4

Linked Data

• dbSNP Id: rs1278754193
• MyVariant Identifiers: chr1:g.173156703G>A (hg19) ; chr1:g.173187564G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173187564G>A , CM000663.2:g.173187564G>A	GRCh38
NC_000001.10:g.173156703G>A , CM000663.1:g.173156703G>A	GRCh37
NC_000001.9:g.171423326G>A	NCBI36
NG_011477.1:g.24769C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.203-699C>T MANE Select	ENSP00000281834.3:n.203-699C>T
ENST00000281834.3:c.203-699C>T	ENSP00000281834.3:n.203-699C>T
ENST00000367718.5:c.53-699C>T	ENSP00000356691.1:n.53-699C>T
NM_001297562.1:c.53-699C>T	NP_001284491.1:n.53-699C>T
NM_003326.4:c.203-699C>T	NP_003317.1:n.203-699C>T
XM_011509964.1:c.275-699C>T	XP_011508266.1:n.275-699C>T
XM_011509964.2:c.491-699C>T	XP_011508266.2:n.491-699C>T
XM_017002228.1:c.299-699C>T	XP_016857717.1:n.299-699C>T
XM_017002229.1:c.236-699C>T	XP_016857718.1:n.236-699C>T
XM_017002230.1:c.230-699C>T	XP_016857719.1:n.230-699C>T
NM_003326.5:c.203-699C>T MANE Select	NP_003317.1:n.203-699C>T
NM_001297562.2:c.53-699C>T	NP_001284491.1:n.53-699C>T