Canonical Allele Identifier: CA858979266
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1230023577
MyVariant Identifiers: chr9:g.117566366A>T (hg19) chr9:g.114804086A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114804086A>T , CM000671.2:g.114804086A>T GRCh38
NC_000009.11:g.117566366A>T , CM000671.1:g.117566366A>T GRCh37
NC_000009.10:g.116606187A>T NCBI36
NG_011488.2:g.7043T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.210+1717T>A MANE Select ENSP00000363157.3:n.210+1717T>A
ENST00000374045.4:c.210+1717T>A ENSP00000363157.3:n.210+1717T>A
NM_005118.3:c.210+1717T>A NP_005109.2:n.210+1717T>A
NM_005118.4:c.210+1717T>A MANE Select NP_005109.2:n.210+1717T>A
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