Canonical Allele Identifier: CA2117834814

Gene: TNFSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108285104T= , CM000675.2:g.108285104T=	GRCh38
NC_000013.10:g.108937452T= , CM000675.1:g.108937452T=	GRCh37
NC_000013.9:g.107735453T=	NCBI36
NG_029524.1:g.20476T=

Transcript Alleles

HGVS	Amino-acid Change
NM_006573.5:c.425-1699T= MANE Select	NP_006564.1:n.425-1699T=
ENST00000375887.9:c.425-1699T= MANE Select	ENSP00000365048.3:n.425-1699T=
NM_001145645.2:c.424+14680T=	NP_001139117.1:n.424+14680T=
NM_006573.4:c.425-1699T=	NP_006564.1:n.425-1699T=
ENST00000375887.8:c.425-1699T=	ENSP00000365048.3:n.425-1699T=
ENST00000430559.5:c.424+14680T=	ENSP00000389540.1:n.424+14680T=
ENST00000479435.1:n.199-1699T=
ENST00000542136.1:c.425-1699T=	ENSP00000445334.1:n.425-1699T=
XM_005254029.3:c.425-1699T=	XP_005254086.1:n.425-1699T=
XR_001749468.1:n.2081-1699T=
XR_429277.2:n.786+3292A=