Canonical Allele Identifier: CA1874001241
Gene: TNFSF15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.114796293G= , CM000671.2:g.114796293G= GRCh38
NC_000009.11:g.117558573G= , CM000671.1:g.117558573G= GRCh37
NC_000009.10:g.116598394G= NCBI36
NG_011488.2:g.14836C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374045.5:c.211-2725C= MANE Select ENSP00000363157.3:n.211-2725C=
ENST00000374045.4:c.211-2725C= ENSP00000363157.3:n.211-2725C=
NM_005118.3:c.211-2725C= NP_005109.2:n.211-2725C=
NM_005118.4:c.211-2725C= MANE Select NP_005109.2:n.211-2725C=