Canonical Allele Identifier: CA2250305171

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948961C= , CM000679.2:g.16948961C=	GRCh38
NC_000017.10:g.16852275C= , CM000679.1:g.16852275C=	GRCh37
NC_000017.9:g.16793000C=	NCBI36
NG_007281.1:g.28128G= , LRG_120:g.28128G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.222G= MANE Select	ENSP00000261652.2:p.Glu74=
ENST00000261652.6:c.222G=	ENSP00000261652.2:p.Glu74=
ENST00000579315.5:c.222G=	ENSP00000464069.1:p.Glu74=
ENST00000581616.2:n.225G=
ENST00000582931.5:n.126G=
ENST00000583789.1:c.84G=	ENSP00000462952.1:p.Glu28=
ENST00000584950.5:c.84G=	ENSP00000463582.1:p.Glu28=
NM_012452.2:c.222G= , LRG_120t1:c.222G=	NP_036584.1:p.Glu74=
NM_012452.3:c.222G= MANE Select	NP_036584.1:p.Glu74=