Canonical Allele Identifier: CA858969395
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1364055852
gnomAD v3: 9-114785354-T-A
gnomAD v4: 9-114785354-T-A
MyVariant Identifiers: chr9:g.117547634T>A (hg19) chr9:g.114785354T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785354T>A , CM000671.2:g.114785354T>A GRCh38
NC_000009.11:g.117547634T>A , CM000671.1:g.117547634T>A GRCh37
NC_000009.10:g.116587455T>A NCBI36
NG_011488.2:g.25775A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*5098A>T MANE Select ENSP00000363157.3:n.*5098A>T
ENST00000374045.4:c.*5098A>T ENSP00000363157.3:n.*5098A>T
NM_001204344.1:c.5677A>T NP_001191273.1:n.5677A>T
NM_005118.3:c.*5098A>T NP_005109.2:n.*5098A>T
NM_005118.4:c.*5098A>T MANE Select NP_005109.2:n.*5098A>T
Search 100 bp 5'
Search 100 bp 3'