Canonical Allele Identifier: CA198900169
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs968810809
gnomAD v3: 9-114796467-C-T
gnomAD v4: 9-114796467-C-T
MyVariant Identifiers: chr9:g.117558747C>T (hg19) chr9:g.114796467C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796467C>T , CM000671.2:g.114796467C>T GRCh38
NC_000009.11:g.117558747C>T , CM000671.1:g.117558747C>T GRCh37
NC_000009.10:g.116598568C>T NCBI36
NG_011488.2:g.14662G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000374045.5:c.211-2899G>A MANE Select ENSP00000363157.3:n.211-2899G>A
ENST00000374045.4:c.211-2899G>A ENSP00000363157.3:n.211-2899G>A
NM_005118.3:c.211-2899G>A NP_005109.2:n.211-2899G>A
NM_005118.4:c.211-2899G>A MANE Select NP_005109.2:n.211-2899G>A
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