Canonical Allele Identifier: CA1009207548
Gene: TNFSF4 HGNC NCBI

Linked Data

dbSNP Id: rs1650210041
gnomAD v3: 1-173206739-C-T
gnomAD v4: 1-173206739-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173206739C>T , CM000663.2:g.173206739C>T GRCh38
NC_000001.10:g.173175878C>T , CM000663.1:g.173175878C>T GRCh37
NC_000001.9:g.171442501C>T NCBI36
NG_011477.1:g.5594G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000281834.4:c.153+285G>A MANE Select ENSP00000281834.3:n.153+285G>A
ENST00000281834.3:c.153+285G>A ENSP00000281834.3:n.153+285G>A
NM_003326.4:c.153+285G>A NP_003317.1:n.153+285G>A
XM_011509964.1:c.225+285G>A XP_011508266.1:n.225+285G>A
XM_011509964.2:c.441+285G>A XP_011508266.2:n.441+285G>A
XM_017002228.1:c.-1004G>A XP_016857717.1:n.-1004G>A
XM_017002229.1:c.186+285G>A XP_016857718.1:n.186+285G>A
XM_017002230.1:c.180+285G>A XP_016857719.1:n.180+285G>A
NM_003326.5:c.153+285G>A MANE Select NP_003317.1:n.153+285G>A
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