Canonical Allele Identifier: CA33035449

Gene: TNFSF4

Linked Data

• dbSNP Id: rs909866003
• gnomAD v3: 1-173187302-C-A
• gnomAD v4: 1-173187302-C-A
• MyVariant Identifiers: chr1:g.173156441C>A (hg19) ; chr1:g.173187302C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173187302C>A , CM000663.2:g.173187302C>A	GRCh38
NC_000001.10:g.173156441C>A , CM000663.1:g.173156441C>A	GRCh37
NC_000001.9:g.171423064C>A	NCBI36
NG_011477.1:g.25031G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.203-437G>T MANE Select	ENSP00000281834.3:n.203-437G>T
ENST00000281834.3:c.203-437G>T	ENSP00000281834.3:n.203-437G>T
ENST00000367718.5:c.53-437G>T	ENSP00000356691.1:n.53-437G>T
NM_001297562.1:c.53-437G>T	NP_001284491.1:n.53-437G>T
NM_003326.4:c.203-437G>T	NP_003317.1:n.203-437G>T
XM_011509964.1:c.275-437G>T	XP_011508266.1:n.275-437G>T
XM_011509964.2:c.491-437G>T	XP_011508266.2:n.491-437G>T
XM_017002228.1:c.299-437G>T	XP_016857717.1:n.299-437G>T
XM_017002229.1:c.236-437G>T	XP_016857718.1:n.236-437G>T
XM_017002230.1:c.230-437G>T	XP_016857719.1:n.230-437G>T
NM_003326.5:c.203-437G>T MANE Select	NP_003317.1:n.203-437G>T
NM_001297562.2:c.53-437G>T	NP_001284491.1:n.53-437G>T