Canonical Allele Identifier: CA33035435
Gene: TNFSF4 HGNC NCBI

Linked Data

dbSNP Id: rs3861950
gnomAD v2: 1-173156292-T-C
gnomAD v3: 1-173187153-T-C
gnomAD v4: 1-173187153-T-C
MyVariant Identifiers: chr1:g.173156292T>C (hg19) chr1:g.173187153T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173187153T>C , CM000663.2:g.173187153T>C GRCh38
NC_000001.10:g.173156292T>C , CM000663.1:g.173156292T>C GRCh37
NC_000001.9:g.171422915T>C NCBI36
NG_011477.1:g.25180A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000281834.4:c.203-288A>G MANE Select ENSP00000281834.3:n.203-288A>G
ENST00000281834.3:c.203-288A>G ENSP00000281834.3:n.203-288A>G
ENST00000367718.5:c.53-288A>G ENSP00000356691.1:n.53-288A>G
NM_001297562.1:c.53-288A>G NP_001284491.1:n.53-288A>G
NM_003326.4:c.203-288A>G NP_003317.1:n.203-288A>G
XM_011509964.1:c.275-288A>G XP_011508266.1:n.275-288A>G
XM_011509964.2:c.491-288A>G XP_011508266.2:n.491-288A>G
XM_017002228.1:c.299-288A>G XP_016857717.1:n.299-288A>G
XM_017002229.1:c.236-288A>G XP_016857718.1:n.236-288A>G
XM_017002230.1:c.230-288A>G XP_016857719.1:n.230-288A>G
NM_003326.5:c.203-288A>G MANE Select NP_003317.1:n.203-288A>G
NM_001297562.2:c.53-288A>G NP_001284491.1:n.53-288A>G
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