Canonical Allele Identifier: CA2250304839

Gene: TNFRSF13B

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948876_16948877delinsAG , CM000679.2:g.16948876_16948877delinsAG	GRCh38
NC_000017.10:g.16852190_16852191delinsAG , CM000679.1:g.16852190_16852191delinsAG	GRCh37
NC_000017.9:g.16792915_16792916delinsAG	NCBI36
NG_007281.1:g.28212_28213delinsCT , LRG_120:g.28212_28213delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.306_307delinsCT MANE Select	ENSP00000261652.2:p.Tyr102=
ENST00000261652.6:c.306_307delinsCT	ENSP00000261652.2:p.Tyr102=
ENST00000579315.5:c.306_307delinsCT	ENSP00000464069.1:p.Tyr102=
ENST00000581616.2:n.309_310delinsCT
ENST00000582931.5:n.210_211delinsCT
ENST00000583789.1:c.168_169delinsCT	ENSP00000462952.1:p.Tyr56=
ENST00000584950.5:c.168_169delinsCT	ENSP00000463582.1:p.Tyr56=
NM_012452.2:c.306_307delinsCT , LRG_120t1:c.306_307delinsCT	NP_036584.1:p.Tyr102=
NM_012452.3:c.306_307delinsCT MANE Select	NP_036584.1:p.Tyr102=