Canonical Allele Identifier: CA2636330361

Gene: TNFRSF13B

Linked Data

• gnomAD v4: 17-16949077-TACAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16949078_16949081del , CM000679.2:g.16949078_16949081del	GRCh38
NC_000017.10:g.16852392_16852395del , CM000679.1:g.16852392_16852395del	GRCh37
NC_000017.9:g.16793117_16793120del	NCBI36
NG_007281.1:g.28008_28011del , LRG_120:g.28008_28011del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.200-98_200-95del MANE Select	ENSP00000261652.2:n.200-98_200-95del
ENST00000261652.6:c.200-98_200-95del	ENSP00000261652.2:n.200-98_200-95del
ENST00000579315.5:c.200-98_200-95del	ENSP00000464069.1:n.200-98_200-95del
ENST00000581616.2:n.203-98_203-95del
ENST00000582931.5:n.104-98_104-95del
ENST00000583789.1:c.62-98_62-95del	ENSP00000462952.1:n.62-98_62-95del
ENST00000584950.5:c.62-98_62-95del	ENSP00000463582.1:n.62-98_62-95del
NM_012452.2:c.200-98_200-95del , LRG_120t1:c.200-98_200-95del	NP_036584.1:n.200-98_200-95del
NM_012452.3:c.200-98_200-95del MANE Select	NP_036584.1:n.200-98_200-95del