Canonical Allele Identifier: CA198899008
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs779960072
MyVariant Identifiers: chr9:g.117547696A>G (hg19) chr9:g.114785416A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785416A>G , CM000671.2:g.114785416A>G GRCh38
NC_000009.11:g.117547696A>G , CM000671.1:g.117547696A>G GRCh37
NC_000009.10:g.116587517A>G NCBI36
NG_011488.2:g.25713T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*5036T>C MANE Select ENSP00000363157.3:n.*5036T>C
ENST00000374045.4:c.*5036T>C ENSP00000363157.3:n.*5036T>C
NM_001204344.1:c.5615T>C NP_001191273.1:n.5615T>C
NM_005118.3:c.*5036T>C NP_005109.2:n.*5036T>C
NM_005118.4:c.*5036T>C MANE Select NP_005109.2:n.*5036T>C
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