Canonical Allele Identifier: CA2250304151

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948689G= , CM000679.2:g.16948689G=	GRCh38
NC_000017.10:g.16852003G= , CM000679.1:g.16852003G=	GRCh37
NC_000017.9:g.16792728G=	NCBI36
NG_007281.1:g.28400C= , LRG_120:g.28400C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.445+49C= MANE Select	ENSP00000261652.2:n.445+49C=
ENST00000261652.6:c.445+49C=	ENSP00000261652.2:n.445+49C=
ENST00000579315.5:c.445+49C=	ENSP00000464069.1:n.445+49C=
ENST00000581616.2:n.448+49C=
ENST00000582931.5:n.349+49C=
ENST00000583789.1:c.307+49C=	ENSP00000462952.1:n.307+49C=
ENST00000584950.5:c.307+49C=	ENSP00000463582.1:n.307+49C=
NM_012452.2:c.445+49C= , LRG_120t1:c.445+49C=	NP_036584.1:n.445+49C=
NM_012452.3:c.445+49C= MANE Select	NP_036584.1:n.445+49C=