Canonical Allele Identifier: CA2117837265

Gene: TNFSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.108290440G= , CM000675.2:g.108290440G=	GRCh38
NC_000013.10:g.108942788G= , CM000675.1:g.108942788G=	GRCh37
NC_000013.9:g.107740789G=	NCBI36
NG_029524.1:g.25812G=

Transcript Alleles

HGVS	Amino-acid Change
NM_006573.5:c.481+3581G= MANE Select	NP_006564.1:n.481+3581G=
ENST00000375887.9:c.481+3581G= MANE Select	ENSP00000365048.3:n.481+3581G=
NM_001145645.2:c.425-12813G=	NP_001139117.1:n.425-12813G=
NM_006573.4:c.481+3581G=	NP_006564.1:n.481+3581G=
ENST00000375887.8:c.481+3581G=	ENSP00000365048.3:n.481+3581G=
ENST00000430559.5:c.425-12813G=	ENSP00000389540.1:n.425-12813G=
ENST00000479435.1:n.255+3581G=
ENST00000542136.1:c.481+3581G=	ENSP00000445334.1:n.481+3581G=
XM_005254029.3:c.481+3581G=	XP_005254086.1:n.481+3581G=
XR_001749468.1:n.2137+3581G=
XR_429277.2:n.782+1506C=