Canonical Allele Identifier: CA1874007068
Gene: TNFSF15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114804138C= , CM000671.2:g.114804138C= GRCh38
NC_000009.11:g.117566418C= , CM000671.1:g.117566418C= GRCh37
NC_000009.10:g.116606239C= NCBI36
NG_011488.2:g.6991G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.210+1665G= MANE Select ENSP00000363157.3:n.210+1665G=
ENST00000374045.4:c.210+1665G= ENSP00000363157.3:n.210+1665G=
NM_005118.3:c.210+1665G= NP_005109.2:n.210+1665G=
NM_005118.4:c.210+1665G= MANE Select NP_005109.2:n.210+1665G=