Canonical Allele Identifier: CA2250304962

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948904A= , CM000679.2:g.16948904A=	GRCh38
NC_000017.10:g.16852218A= , CM000679.1:g.16852218A=	GRCh37
NC_000017.9:g.16792943A=	NCBI36
NG_007281.1:g.28185T= , LRG_120:g.28185T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.279T= MANE Select	ENSP00000261652.2:p.Cys93=
ENST00000261652.6:c.279T=	ENSP00000261652.2:p.Cys93=
ENST00000579315.5:c.279T=	ENSP00000464069.1:p.Cys93=
ENST00000581616.2:n.282T=
ENST00000582931.5:n.183T=
ENST00000583789.1:c.141T=	ENSP00000462952.1:p.Cys47=
ENST00000584950.5:c.141T=	ENSP00000463582.1:p.Cys47=
NM_012452.2:c.279T= , LRG_120t1:c.279T=	NP_036584.1:p.Cys93=
NM_012452.3:c.279T= MANE Select	NP_036584.1:p.Cys93=