Canonical Allele Identifier: CA891276776

Gene: TNFSF4

Linked Data

• dbSNP Id: rs1303324551
• gnomAD v3: 1-173206732-G-A
• gnomAD v4: 1-173206732-G-A
• MyVariant Identifiers: chr1:g.173175871G>A (hg19) ; chr1:g.173206732G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173206732G>A , CM000663.2:g.173206732G>A	GRCh38
NC_000001.10:g.173175871G>A , CM000663.1:g.173175871G>A	GRCh37
NC_000001.9:g.171442494G>A	NCBI36
NG_011477.1:g.5601C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000281834.4:c.153+292C>T MANE Select	ENSP00000281834.3:n.153+292C>T
ENST00000281834.3:c.153+292C>T	ENSP00000281834.3:n.153+292C>T
NM_003326.4:c.153+292C>T	NP_003317.1:n.153+292C>T
XM_011509964.1:c.225+292C>T	XP_011508266.1:n.225+292C>T
XM_011509964.2:c.441+292C>T	XP_011508266.2:n.441+292C>T
XM_017002228.1:c.-997C>T	XP_016857717.1:n.-997C>T
XM_017002229.1:c.186+292C>T	XP_016857718.1:n.186+292C>T
XM_017002230.1:c.180+292C>T	XP_016857719.1:n.180+292C>T
NM_003326.5:c.153+292C>T MANE Select	NP_003317.1:n.153+292C>T