Canonical Allele Identifier: CA2250304965

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948908A= , CM000679.2:g.16948908A=	GRCh38
NC_000017.10:g.16852222A= , CM000679.1:g.16852222A=	GRCh37
NC_000017.9:g.16792947A=	NCBI36
NG_007281.1:g.28181T= , LRG_120:g.28181T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.275T= MANE Select	ENSP00000261652.2:p.Ile92=
ENST00000261652.6:c.275T=	ENSP00000261652.2:p.Ile92=
ENST00000579315.5:c.275T=	ENSP00000464069.1:p.Ile92=
ENST00000581616.2:n.278T=
ENST00000582931.5:n.179T=
ENST00000583789.1:c.137T=	ENSP00000462952.1:p.Ile46=
ENST00000584950.5:c.137T=	ENSP00000463582.1:p.Ile46=
NM_012452.2:c.275T= , LRG_120t1:c.275T=	NP_036584.1:p.Ile92=
NM_012452.3:c.275T= MANE Select	NP_036584.1:p.Ile92=