Canonical Allele Identifier: CA33035485

Gene: TNFSF4

Linked Data

• dbSNP Id: rs534264999
• gnomAD v2: 1-173156701-G-C
• gnomAD v3: 1-173187562-G-C
• gnomAD v4: 1-173187562-G-C
• MyVariant Identifiers: chr1:g.173156701G>C (hg19) ; chr1:g.173187562G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173187562G>C , CM000663.2:g.173187562G>C	GRCh38
NC_000001.10:g.173156701G>C , CM000663.1:g.173156701G>C	GRCh37
NC_000001.9:g.171423324G>C	NCBI36
NG_011477.1:g.24771C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.203-697C>G MANE Select	ENSP00000281834.3:n.203-697C>G
ENST00000281834.3:c.203-697C>G	ENSP00000281834.3:n.203-697C>G
ENST00000367718.5:c.53-697C>G	ENSP00000356691.1:n.53-697C>G
NM_001297562.1:c.53-697C>G	NP_001284491.1:n.53-697C>G
NM_003326.4:c.203-697C>G	NP_003317.1:n.203-697C>G
XM_011509964.1:c.275-697C>G	XP_011508266.1:n.275-697C>G
XM_011509964.2:c.491-697C>G	XP_011508266.2:n.491-697C>G
XM_017002228.1:c.299-697C>G	XP_016857717.1:n.299-697C>G
XM_017002229.1:c.236-697C>G	XP_016857718.1:n.236-697C>G
XM_017002230.1:c.230-697C>G	XP_016857719.1:n.230-697C>G
NM_003326.5:c.203-697C>G MANE Select	NP_003317.1:n.203-697C>G
NM_001297562.2:c.53-697C>G	NP_001284491.1:n.53-697C>G