Canonical Allele Identifier: CA2250304872

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948881G= , CM000679.2:g.16948881G=	GRCh38
NC_000017.10:g.16852195G= , CM000679.1:g.16852195G=	GRCh37
NC_000017.9:g.16792920G=	NCBI36
NG_007281.1:g.28208C= , LRG_120:g.28208C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.302C= MANE Select	ENSP00000261652.2:p.Ala101=
ENST00000261652.6:c.302C=	ENSP00000261652.2:p.Ala101=
ENST00000579315.5:c.302C=	ENSP00000464069.1:p.Ala101=
ENST00000581616.2:n.305C=
ENST00000582931.5:n.206C=
ENST00000583789.1:c.164C=	ENSP00000462952.1:p.Ala55=
ENST00000584950.5:c.164C=	ENSP00000463582.1:p.Ala55=
NM_012452.2:c.302C= , LRG_120t1:c.302C=	NP_036584.1:p.Ala101=
NM_012452.3:c.302C= MANE Select	NP_036584.1:p.Ala101=