Canonical Allele Identifier: CA891276775

Gene: TNFSF4

Linked Data

• dbSNP Id: rs1331432627
• gnomAD v3: 1-173206707-T-C
• gnomAD v4: 1-173206707-T-C
• MyVariant Identifiers: chr1:g.173175846T>C (hg19) ; chr1:g.173206707T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173206707T>C , CM000663.2:g.173206707T>C	GRCh38
NC_000001.10:g.173175846T>C , CM000663.1:g.173175846T>C	GRCh37
NC_000001.9:g.171442469T>C	NCBI36
NG_011477.1:g.5626A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000281834.4:c.153+317A>G MANE Select	ENSP00000281834.3:n.153+317A>G
ENST00000281834.3:c.153+317A>G	ENSP00000281834.3:n.153+317A>G
NM_003326.4:c.153+317A>G	NP_003317.1:n.153+317A>G
XM_011509964.1:c.225+317A>G	XP_011508266.1:n.225+317A>G
XM_011509964.2:c.441+317A>G	XP_011508266.2:n.441+317A>G
XM_017002228.1:c.-972A>G	XP_016857717.1:n.-972A>G
XM_017002229.1:c.186+317A>G	XP_016857718.1:n.186+317A>G
XM_017002230.1:c.180+317A>G	XP_016857719.1:n.180+317A>G
NM_003326.5:c.153+317A>G MANE Select	NP_003317.1:n.153+317A>G