Canonical Allele Identifier: CA2636330203

Gene: TNFRSF13B

Linked Data

• gnomAD v4: 17-16949026-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16949026_16949027insT , CM000679.2:g.16949026_16949027insT	GRCh38
NC_000017.10:g.16852340_16852341insT , CM000679.1:g.16852340_16852341insT	GRCh37
NC_000017.9:g.16793065_16793066insT	NCBI36
NG_007281.1:g.28062_28063insA , LRG_120:g.28062_28063insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.200-44_200-43insA MANE Select	ENSP00000261652.2:n.200-44_200-43insA
ENST00000261652.6:c.200-44_200-43insA	ENSP00000261652.2:n.200-44_200-43insA
ENST00000579315.5:c.200-44_200-43insA	ENSP00000464069.1:n.200-44_200-43insA
ENST00000581616.2:n.203-44_203-43insA
ENST00000582931.5:n.104-44_104-43insA
ENST00000583789.1:c.62-44_62-43insA	ENSP00000462952.1:n.62-44_62-43insA
ENST00000584950.5:c.62-44_62-43insA	ENSP00000463582.1:n.62-44_62-43insA
NM_012452.2:c.200-44_200-43insA , LRG_120t1:c.200-44_200-43insA	NP_036584.1:n.200-44_200-43insA
NM_012452.3:c.200-44_200-43insA MANE Select	NP_036584.1:n.200-44_200-43insA