Canonical Allele Identifier: CA198899021
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs371434038
MyVariant Identifiers: chr9:g.117547823C>T (hg19) chr9:g.114785543C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785543C>T , CM000671.2:g.114785543C>T GRCh38
NC_000009.11:g.117547823C>T , CM000671.1:g.117547823C>T GRCh37
NC_000009.10:g.116587644C>T NCBI36
NG_011488.2:g.25586G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*4909G>A MANE Select ENSP00000363157.3:n.*4909G>A
ENST00000374045.4:c.*4909G>A ENSP00000363157.3:n.*4909G>A
NM_001204344.1:c.5488G>A NP_001191273.1:n.5488G>A
NM_005118.3:c.*4909G>A NP_005109.2:n.*4909G>A
NM_005118.4:c.*4909G>A MANE Select NP_005109.2:n.*4909G>A
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