Canonical Allele Identifier: CA2250304194

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948708C= , CM000679.2:g.16948708C=	GRCh38
NC_000017.10:g.16852022C= , CM000679.1:g.16852022C=	GRCh37
NC_000017.9:g.16792747C=	NCBI36
NG_007281.1:g.28381G= , LRG_120:g.28381G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.445+30G= MANE Select	ENSP00000261652.2:n.445+30G=
ENST00000261652.6:c.445+30G=	ENSP00000261652.2:n.445+30G=
ENST00000579315.5:c.445+30G=	ENSP00000464069.1:n.445+30G=
ENST00000581616.2:n.448+30G=
ENST00000582931.5:n.349+30G=
ENST00000583789.1:c.307+30G=	ENSP00000462952.1:n.307+30G=
ENST00000584950.5:c.307+30G=	ENSP00000463582.1:n.307+30G=
NM_012452.2:c.445+30G= , LRG_120t1:c.445+30G=	NP_036584.1:n.445+30G=
NM_012452.3:c.445+30G= MANE Select	NP_036584.1:n.445+30G=