Canonical Allele Identifier: CA1874001341
Gene: TNFSF15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796420T= , CM000671.2:g.114796420T= GRCh38
NC_000009.11:g.117558700T= , CM000671.1:g.117558700T= GRCh37
NC_000009.10:g.116598521T= NCBI36
NG_011488.2:g.14709A=

Transcript Alleles

HGVS Amino-acid change
ENST00000374045.5:c.211-2852A= MANE Select ENSP00000363157.3:n.211-2852A=
ENST00000374045.4:c.211-2852A= ENSP00000363157.3:n.211-2852A=
NM_005118.3:c.211-2852A= NP_005109.2:n.211-2852A=
NM_005118.4:c.211-2852A= MANE Select NP_005109.2:n.211-2852A=