Canonical Allele Identifier: CA2250305231

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948976G= , CM000679.2:g.16948976G=	GRCh38
NC_000017.10:g.16852290G= , CM000679.1:g.16852290G=	GRCh37
NC_000017.9:g.16793015G=	NCBI36
NG_007281.1:g.28113C= , LRG_120:g.28113C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.207C= MANE Select	ENSP00000261652.2:p.Leu69=
ENST00000261652.6:c.207C=	ENSP00000261652.2:p.Leu69=
ENST00000579315.5:c.207C=	ENSP00000464069.1:p.Leu69=
ENST00000581616.2:n.210C=
ENST00000582931.5:n.111C=
ENST00000583789.1:c.69C=	ENSP00000462952.1:p.Leu23=
ENST00000584950.5:c.69C=	ENSP00000463582.1:p.Leu23=
NM_012452.2:c.207C= , LRG_120t1:c.207C=	NP_036584.1:p.Leu69=
NM_012452.3:c.207C= MANE Select	NP_036584.1:p.Leu69=