Canonical Allele Identifier: CA625313747
Gene: TNFRSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1567652308

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948920_16948939del , CM000679.2:g.16948920_16948939del GRCh38
NC_000017.10:g.16852234_16852253del , CM000679.1:g.16852234_16852253del GRCh37
NC_000017.9:g.16792959_16792978del NCBI36
NG_007281.1:g.28152_28171del , LRG_120:g.28152_28171del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.246_265del MANE Select ENSP00000261652.2:p.Leu83CysfsTer9
ENST00000261652.6:c.246_265del ENSP00000261652.2:p.Leu83CysfsTer9
ENST00000579315.5:c.246_265del ENSP00000464069.1:p.Leu83CysfsTer9
ENST00000581616.2:n.249_268del
ENST00000582931.5:n.150_169del
ENST00000583789.1:c.108_127del ENSP00000462952.1:p.Leu37CysfsTer9
ENST00000584950.5:c.108_127del ENSP00000463582.1:p.Leu37CysfsTer9
NM_012452.2:c.246_265del , LRG_120t1:c.246_265del NP_036584.1:p.Leu83CysfsTer9
NM_012452.3:c.246_265del MANE Select NP_036584.1:p.Leu83CysfsTer9