Canonical Allele Identifier: CA527368862

Gene: TNFSF4

Linked Data

• dbSNP Id: rs1469798799
• gnomAD v2: 1-173156480-T-G
• gnomAD v3: 1-173187341-T-G
• gnomAD v4: 1-173187341-T-G
• MyVariant Identifiers: chr1:g.173156480T>G (hg19) ; chr1:g.173187341T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173187341T>G , CM000663.2:g.173187341T>G	GRCh38
NC_000001.10:g.173156480T>G , CM000663.1:g.173156480T>G	GRCh37
NC_000001.9:g.171423103T>G	NCBI36
NG_011477.1:g.24992A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281834.4:c.203-476A>C MANE Select	ENSP00000281834.3:n.203-476A>C
ENST00000281834.3:c.203-476A>C	ENSP00000281834.3:n.203-476A>C
ENST00000367718.5:c.53-476A>C	ENSP00000356691.1:n.53-476A>C
NM_001297562.1:c.53-476A>C	NP_001284491.1:n.53-476A>C
NM_003326.4:c.203-476A>C	NP_003317.1:n.203-476A>C
XM_011509964.1:c.275-476A>C	XP_011508266.1:n.275-476A>C
XM_011509964.2:c.491-476A>C	XP_011508266.2:n.491-476A>C
XM_017002228.1:c.299-476A>C	XP_016857717.1:n.299-476A>C
XM_017002229.1:c.236-476A>C	XP_016857718.1:n.236-476A>C
XM_017002230.1:c.230-476A>C	XP_016857719.1:n.230-476A>C
NM_003326.5:c.203-476A>C MANE Select	NP_003317.1:n.203-476A>C
NM_001297562.2:c.53-476A>C	NP_001284491.1:n.53-476A>C