Canonical Allele Identifier: CA2250293069

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16941910A= , CM000679.2:g.16941910A=	GRCh38
NC_000017.10:g.16845224A= , CM000679.1:g.16845224A=	GRCh37
NC_000017.9:g.16785949A=	NCBI36
NG_007281.1:g.35179T= , LRG_120:g.35179T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.446-1399T= MANE Select	ENSP00000261652.2:n.446-1399T=
ENST00000261652.6:c.446-1399T=	ENSP00000261652.2:n.446-1399T=
ENST00000579315.5:c.445+6828T=	ENSP00000464069.1:n.445+6828T=
ENST00000581616.2:n.449-433T=
ENST00000582931.5:n.349+6828T=
ENST00000583789.1:c.308-1399T=	ENSP00000462952.1:n.308-1399T=
ENST00000584950.5:c.308-1399T=	ENSP00000463582.1:n.308-1399T=
NM_012452.2:c.446-1399T= , LRG_120t1:c.446-1399T=	NP_036584.1:n.446-1399T=
NM_012452.3:c.446-1399T= MANE Select	NP_036584.1:n.446-1399T=