Canonical Allele Identifier: CA858969418
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs1451087390

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785455G>A , CM000671.2:g.114785455G>A GRCh38
NC_000009.11:g.117547735G>A , CM000671.1:g.117547735G>A GRCh37
NC_000009.10:g.116587556G>A NCBI36
NG_011488.2:g.25674C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*4997C>T MANE Select ENSP00000363157.3:n.*4997C>T
ENST00000374045.4:c.*4997C>T ENSP00000363157.3:n.*4997C>T
NM_001204344.1:c.5576C>T NP_001191273.1:n.5576C>T
NM_005118.3:c.*4997C>T NP_005109.2:n.*4997C>T
NM_005118.4:c.*4997C>T MANE Select NP_005109.2:n.*4997C>T