Canonical Allele Identifier: CA2250304197

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948709A= , CM000679.2:g.16948709A=	GRCh38
NC_000017.10:g.16852023A= , CM000679.1:g.16852023A=	GRCh37
NC_000017.9:g.16792748A=	NCBI36
NG_007281.1:g.28380T= , LRG_120:g.28380T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.445+29T= MANE Select	ENSP00000261652.2:n.445+29T=
ENST00000261652.6:c.445+29T=	ENSP00000261652.2:n.445+29T=
ENST00000579315.5:c.445+29T=	ENSP00000464069.1:n.445+29T=
ENST00000581616.2:n.448+29T=
ENST00000582931.5:n.349+29T=
ENST00000583789.1:c.307+29T=	ENSP00000462952.1:n.307+29T=
ENST00000584950.5:c.307+29T=	ENSP00000463582.1:n.307+29T=
NM_012452.2:c.445+29T= , LRG_120t1:c.445+29T=	NP_036584.1:n.445+29T=
NM_012452.3:c.445+29T= MANE Select	NP_036584.1:n.445+29T=