Canonical Allele Identifier: CA2691385644
Gene: TNFSF15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114785547T>A , CM000671.2:g.114785547T>A GRCh38
NC_000009.11:g.117547827T>A , CM000671.1:g.117547827T>A GRCh37
NC_000009.10:g.116587648T>A NCBI36
NG_011488.2:g.25582A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374045.5:c.*4905A>T MANE Select ENSP00000363157.3:n.*4905A>T
ENST00000374045.4:c.*4905A>T ENSP00000363157.3:n.*4905A>T
NM_001204344.1:c.5484A>T NP_001191273.1:n.5484A>T
NM_005118.3:c.*4905A>T NP_005109.2:n.*4905A>T
NM_005118.4:c.*4905A>T MANE Select NP_005109.2:n.*4905A>T