Canonical Allele Identifier: CA2250292826

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16941712T= , CM000679.2:g.16941712T=	GRCh38
NC_000017.10:g.16845026T= , CM000679.1:g.16845026T=	GRCh37
NC_000017.9:g.16785751T=	NCBI36
NG_007281.1:g.35377A= , LRG_120:g.35377A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.446-1201A= MANE Select	ENSP00000261652.2:n.446-1201A=
ENST00000261652.6:c.446-1201A=	ENSP00000261652.2:n.446-1201A=
ENST00000579315.5:c.445+7026A=	ENSP00000464069.1:n.445+7026A=
ENST00000581616.2:n.449-235A=
ENST00000582931.5:n.349+7026A=
ENST00000583789.1:c.308-1201A=	ENSP00000462952.1:n.308-1201A=
ENST00000584950.5:c.308-1201A=	ENSP00000463582.1:n.308-1201A=
NM_012452.2:c.446-1201A= , LRG_120t1:c.446-1201A=	NP_036584.1:n.446-1201A=
NM_012452.3:c.446-1201A= MANE Select	NP_036584.1:n.446-1201A=