Canonical Allele Identifier: CA1874007036
Gene: TNFSF15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114804097T= , CM000671.2:g.114804097T= GRCh38
NC_000009.11:g.117566377T= , CM000671.1:g.117566377T= GRCh37
NC_000009.10:g.116606198T= NCBI36
NG_011488.2:g.7032A=

Transcript Alleles

HGVS Amino-acid change
ENST00000374045.5:c.210+1706A= MANE Select ENSP00000363157.3:n.210+1706A=
ENST00000374045.4:c.210+1706A= ENSP00000363157.3:n.210+1706A=
NM_005118.3:c.210+1706A= NP_005109.2:n.210+1706A=
NM_005118.4:c.210+1706A= MANE Select NP_005109.2:n.210+1706A=