Canonical Allele Identifier: CA891270275

Gene: TNFSF4

Linked Data

• dbSNP Id: rs1240990967
• MyVariant Identifiers: chr1:g.173156201A>G (hg19) ; chr1:g.173187062A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173187062A>G , CM000663.2:g.173187062A>G	GRCh38
NC_000001.10:g.173156201A>G , CM000663.1:g.173156201A>G	GRCh37
NC_000001.9:g.171422824A>G	NCBI36
NG_011477.1:g.25271T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.203-197T>C MANE Select	ENSP00000281834.3:n.203-197T>C
ENST00000281834.3:c.203-197T>C	ENSP00000281834.3:n.203-197T>C
ENST00000367718.5:c.53-197T>C	ENSP00000356691.1:n.53-197T>C
NM_001297562.1:c.53-197T>C	NP_001284491.1:n.53-197T>C
NM_003326.4:c.203-197T>C	NP_003317.1:n.203-197T>C
XM_011509964.1:c.275-197T>C	XP_011508266.1:n.275-197T>C
XM_011509964.2:c.491-197T>C	XP_011508266.2:n.491-197T>C
XM_017002228.1:c.299-197T>C	XP_016857717.1:n.299-197T>C
XM_017002229.1:c.236-197T>C	XP_016857718.1:n.236-197T>C
XM_017002230.1:c.230-197T>C	XP_016857719.1:n.230-197T>C
NM_003326.5:c.203-197T>C MANE Select	NP_003317.1:n.203-197T>C
NM_001297562.2:c.53-197T>C	NP_001284491.1:n.53-197T>C