Canonical Allele Identifier: CA1874001399

Gene: TNFSF15

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.114796500G= , CM000671.2:g.114796500G=	GRCh38
NC_000009.11:g.117558780G= , CM000671.1:g.117558780G=	GRCh37
NC_000009.10:g.116598601G=	NCBI36
NG_011488.2:g.14629C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374045.5:c.211-2932C= MANE Select	ENSP00000363157.3:n.211-2932C=
ENST00000374045.4:c.211-2932C=	ENSP00000363157.3:n.211-2932C=
NM_005118.3:c.211-2932C=	NP_005109.2:n.211-2932C=
NM_005118.4:c.211-2932C= MANE Select	NP_005109.2:n.211-2932C=