Canonical Allele Identifier: CA2250305079

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948942G= , CM000679.2:g.16948942G=	GRCh38
NC_000017.10:g.16852256G= , CM000679.1:g.16852256G=	GRCh37
NC_000017.9:g.16792981G=	NCBI36
NG_007281.1:g.28147C= , LRG_120:g.28147C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.241C= MANE Select	ENSP00000261652.2:p.His81=
ENST00000261652.6:c.241C=	ENSP00000261652.2:p.His81=
ENST00000579315.5:c.241C=	ENSP00000464069.1:p.His81=
ENST00000581616.2:n.244C=
ENST00000582931.5:n.145C=
ENST00000583789.1:c.103C=	ENSP00000462952.1:p.His35=
ENST00000584950.5:c.103C=	ENSP00000463582.1:p.His35=
NM_012452.2:c.241C= , LRG_120t1:c.241C=	NP_036584.1:p.His81=
NM_012452.3:c.241C= MANE Select	NP_036584.1:p.His81=