Canonical Allele Identifier: CA1009205493

Gene: TNFSF4

Linked Data

• dbSNP Id: rs1649934869
• gnomAD v3: 1-173201391-G-T
• gnomAD v4: 1-173201391-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173201391G>T , CM000663.2:g.173201391G>T	GRCh38
NC_000001.10:g.173170530G>T , CM000663.1:g.173170530G>T	GRCh37
NC_000001.9:g.171437153G>T	NCBI36
NG_011477.1:g.10942C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000281834.4:c.153+5633C>A MANE Select	ENSP00000281834.3:n.153+5633C>A
ENST00000281834.3:c.153+5633C>A	ENSP00000281834.3:n.153+5633C>A
ENST00000367718.5:c.3+3920C>A	ENSP00000356691.1:n.3+3920C>A
ENST00000488053.1:n.414+3920C>A
NM_001297562.1:c.3+3920C>A	NP_001284491.1:n.3+3920C>A
NM_003326.4:c.153+5633C>A	NP_003317.1:n.153+5633C>A
XM_011509964.1:c.225+5633C>A	XP_011508266.1:n.225+5633C>A
XM_011509964.2:c.441+5633C>A	XP_011508266.2:n.441+5633C>A
XM_017002228.1:c.249+4096C>A	XP_016857717.1:n.249+4096C>A
XM_017002229.1:c.186+5633C>A	XP_016857718.1:n.186+5633C>A
XM_017002230.1:c.180+5633C>A	XP_016857719.1:n.180+5633C>A
NM_003326.5:c.153+5633C>A MANE Select	NP_003317.1:n.153+5633C>A
NM_001297562.2:c.3+3920C>A	NP_001284491.1:n.3+3920C>A