Canonical Allele Identifier: CA2250304148

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948688C= , CM000679.2:g.16948688C=	GRCh38
NC_000017.10:g.16852002C= , CM000679.1:g.16852002C=	GRCh37
NC_000017.9:g.16792727C=	NCBI36
NG_007281.1:g.28401G= , LRG_120:g.28401G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.445+50G= MANE Select	ENSP00000261652.2:n.445+50G=
ENST00000261652.6:c.445+50G=	ENSP00000261652.2:n.445+50G=
ENST00000579315.5:c.445+50G=	ENSP00000464069.1:n.445+50G=
ENST00000581616.2:n.448+50G=
ENST00000582931.5:n.349+50G=
ENST00000583789.1:c.307+50G=	ENSP00000462952.1:n.307+50G=
ENST00000584950.5:c.307+50G=	ENSP00000463582.1:n.307+50G=
NM_012452.2:c.445+50G= , LRG_120t1:c.445+50G=	NP_036584.1:n.445+50G=
NM_012452.3:c.445+50G= MANE Select	NP_036584.1:n.445+50G=