Canonical Allele Identifier: CA858969388
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1327860737
MyVariant Identifiers: chr9:g.117547606T>C (hg19) chr9:g.114785326T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785326T>C , CM000671.2:g.114785326T>C GRCh38
NC_000009.11:g.117547606T>C , CM000671.1:g.117547606T>C GRCh37
NC_000009.10:g.116587427T>C NCBI36
NG_011488.2:g.25803A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374045.5:c.*5126A>G MANE Select ENSP00000363157.3:n.*5126A>G
ENST00000374045.4:c.*5126A>G ENSP00000363157.3:n.*5126A>G
NM_001204344.1:c.5705A>G NP_001191273.1:n.5705A>G
NM_005118.3:c.*5126A>G NP_005109.2:n.*5126A>G
NM_005118.4:c.*5126A>G MANE Select NP_005109.2:n.*5126A>G
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