Canonical Allele Identifier: CA1207645378
Gene: TNFSF4 HGNC NCBI

Linked Data

dbSNP Id: rs1649274710

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173187343G>C , CM000663.2:g.173187343G>C GRCh38
NC_000001.10:g.173156482G>C , CM000663.1:g.173156482G>C GRCh37
NC_000001.9:g.171423105G>C NCBI36
NG_011477.1:g.24990C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000281834.4:c.203-478C>G MANE Select ENSP00000281834.3:n.203-478C>G
ENST00000281834.3:c.203-478C>G ENSP00000281834.3:n.203-478C>G
ENST00000367718.5:c.53-478C>G ENSP00000356691.1:n.53-478C>G
NM_001297562.1:c.53-478C>G NP_001284491.1:n.53-478C>G
NM_003326.4:c.203-478C>G NP_003317.1:n.203-478C>G
XM_011509964.1:c.275-478C>G XP_011508266.1:n.275-478C>G
XM_011509964.2:c.491-478C>G XP_011508266.2:n.491-478C>G
XM_017002228.1:c.299-478C>G XP_016857717.1:n.299-478C>G
XM_017002229.1:c.236-478C>G XP_016857718.1:n.236-478C>G
XM_017002230.1:c.230-478C>G XP_016857719.1:n.230-478C>G
NM_003326.5:c.203-478C>G MANE Select NP_003317.1:n.203-478C>G
NM_001297562.2:c.53-478C>G NP_001284491.1:n.53-478C>G