Canonical Allele Identifier: CA1874007013
Gene: TNFSF15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114804085C= , CM000671.2:g.114804085C= GRCh38
NC_000009.11:g.117566365C= , CM000671.1:g.117566365C= GRCh37
NC_000009.10:g.116606186C= NCBI36
NG_011488.2:g.7044G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.210+1718G= MANE Select ENSP00000363157.3:n.210+1718G=
ENST00000374045.4:c.210+1718G= ENSP00000363157.3:n.210+1718G=
NM_005118.3:c.210+1718G= NP_005109.2:n.210+1718G=
NM_005118.4:c.210+1718G= MANE Select NP_005109.2:n.210+1718G=