Canonical Allele Identifier: CA1128363703
Gene: TNFSF15 HGNC NCBI

Linked Data

dbSNP Id: rs371434038

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785543C>A , CM000671.2:g.114785543C>A GRCh38
NC_000009.11:g.117547823C>A , CM000671.1:g.117547823C>A GRCh37
NC_000009.10:g.116587644C>A NCBI36
NG_011488.2:g.25586G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.*4909G>T MANE Select ENSP00000363157.3:n.*4909G>T
ENST00000374045.4:c.*4909G>T ENSP00000363157.3:n.*4909G>T
NM_001204344.1:c.5488G>T NP_001191273.1:n.5488G>T
NM_005118.3:c.*4909G>T NP_005109.2:n.*4909G>T
NM_005118.4:c.*4909G>T MANE Select NP_005109.2:n.*4909G>T