Canonical Allele Identifier: CA891275032

Gene: TNFSF4

Linked Data

• dbSNP Id: rs1469961427
• gnomAD v3: 1-173201401-C-A
• gnomAD v4: 1-173201401-C-A
• MyVariant Identifiers: chr1:g.173170540C>A (hg19) ; chr1:g.173201401C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173201401C>A , CM000663.2:g.173201401C>A	GRCh38
NC_000001.10:g.173170540C>A , CM000663.1:g.173170540C>A	GRCh37
NC_000001.9:g.171437163C>A	NCBI36
NG_011477.1:g.10932G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000281834.4:c.153+5623G>T MANE Select	ENSP00000281834.3:n.153+5623G>T
ENST00000281834.3:c.153+5623G>T	ENSP00000281834.3:n.153+5623G>T
ENST00000367718.5:c.3+3910G>T	ENSP00000356691.1:n.3+3910G>T
ENST00000488053.1:n.414+3910G>T
NM_001297562.1:c.3+3910G>T	NP_001284491.1:n.3+3910G>T
NM_003326.4:c.153+5623G>T	NP_003317.1:n.153+5623G>T
XM_011509964.1:c.225+5623G>T	XP_011508266.1:n.225+5623G>T
XM_011509964.2:c.441+5623G>T	XP_011508266.2:n.441+5623G>T
XM_017002228.1:c.249+4086G>T	XP_016857717.1:n.249+4086G>T
XM_017002229.1:c.186+5623G>T	XP_016857718.1:n.186+5623G>T
XM_017002230.1:c.180+5623G>T	XP_016857719.1:n.180+5623G>T
NM_003326.5:c.153+5623G>T MANE Select	NP_003317.1:n.153+5623G>T
NM_001297562.2:c.3+3910G>T	NP_001284491.1:n.3+3910G>T