Canonical Allele Identifier: CA913346635

Gene: TNFSF4

Linked Data

• dbSNP Id: rs1557887677
• gnomAD v2: 1-173175861-A-G
• gnomAD v3: 1-173206722-A-G
• gnomAD v4: 1-173206722-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173206722A>G , CM000663.2:g.173206722A>G	GRCh38
NC_000001.10:g.173175861A>G , CM000663.1:g.173175861A>G	GRCh37
NC_000001.9:g.171442484A>G	NCBI36
NG_011477.1:g.5611T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000281834.4:c.153+302T>C MANE Select	ENSP00000281834.3:n.153+302T>C
ENST00000281834.3:c.153+302T>C	ENSP00000281834.3:n.153+302T>C
NM_003326.4:c.153+302T>C	NP_003317.1:n.153+302T>C
XM_011509964.1:c.225+302T>C	XP_011508266.1:n.225+302T>C
XM_011509964.2:c.441+302T>C	XP_011508266.2:n.441+302T>C
XM_017002228.1:c.-987T>C	XP_016857717.1:n.-987T>C
XM_017002229.1:c.186+302T>C	XP_016857718.1:n.186+302T>C
XM_017002230.1:c.180+302T>C	XP_016857719.1:n.180+302T>C
NM_003326.5:c.153+302T>C MANE Select	NP_003317.1:n.153+302T>C