Canonical Allele Identifier: CA2250305161

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948958T= , CM000679.2:g.16948958T=	GRCh38
NC_000017.10:g.16852272T= , CM000679.1:g.16852272T=	GRCh37
NC_000017.9:g.16792997T=	NCBI36
NG_007281.1:g.28131A= , LRG_120:g.28131A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.225A= MANE Select	ENSP00000261652.2:p.Gln75=
ENST00000261652.6:c.225A=	ENSP00000261652.2:p.Gln75=
ENST00000579315.5:c.225A=	ENSP00000464069.1:p.Gln75=
ENST00000581616.2:n.228A=
ENST00000582931.5:n.129A=
ENST00000583789.1:c.87A=	ENSP00000462952.1:p.Gln29=
ENST00000584950.5:c.87A=	ENSP00000463582.1:p.Gln29=
NM_012452.2:c.225A= , LRG_120t1:c.225A=	NP_036584.1:p.Gln75=
NM_012452.3:c.225A= MANE Select	NP_036584.1:p.Gln75=