Canonical Allele Identifier: CA1874001346
Gene: TNFSF15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796424G= , CM000671.2:g.114796424G= GRCh38
NC_000009.11:g.117558704G= , CM000671.1:g.117558704G= GRCh37
NC_000009.10:g.116598525G= NCBI36
NG_011488.2:g.14705C=

Transcript Alleles

HGVS Amino-acid change
ENST00000374045.5:c.211-2856C= MANE Select ENSP00000363157.3:n.211-2856C=
ENST00000374045.4:c.211-2856C= ENSP00000363157.3:n.211-2856C=
NM_005118.3:c.211-2856C= NP_005109.2:n.211-2856C=
NM_005118.4:c.211-2856C= MANE Select NP_005109.2:n.211-2856C=