Canonical Allele Identifier: CA858975408
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1433246540
gnomAD v3: 9-114796413-A-C
gnomAD v4: 9-114796413-A-C
MyVariant Identifiers: chr9:g.117558693A>C (hg19) chr9:g.114796413A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796413A>C , CM000671.2:g.114796413A>C GRCh38
NC_000009.11:g.117558693A>C , CM000671.1:g.117558693A>C GRCh37
NC_000009.10:g.116598514A>C NCBI36
NG_011488.2:g.14716T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000374045.5:c.211-2845T>G MANE Select ENSP00000363157.3:n.211-2845T>G
ENST00000374045.4:c.211-2845T>G ENSP00000363157.3:n.211-2845T>G
NM_005118.3:c.211-2845T>G NP_005109.2:n.211-2845T>G
NM_005118.4:c.211-2845T>G MANE Select NP_005109.2:n.211-2845T>G
Search 100 bp 5'
Search 100 bp 3'