Canonical Allele Identifier: CA1874007109
Gene: TNFSF15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114804200T= , CM000671.2:g.114804200T= GRCh38
NC_000009.11:g.117566480T= , CM000671.1:g.117566480T= GRCh37
NC_000009.10:g.116606301T= NCBI36
NG_011488.2:g.6929A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.210+1603A= MANE Select ENSP00000363157.3:n.210+1603A=
ENST00000374045.4:c.210+1603A= ENSP00000363157.3:n.210+1603A=
NM_005118.3:c.210+1603A= NP_005109.2:n.210+1603A=
NM_005118.4:c.210+1603A= MANE Select NP_005109.2:n.210+1603A=