Canonical Allele Identifier: CA726572785

Gene: TNFRSF13B

Linked Data

• dbSNP Id: rs1259456050
• gnomAD v3: 17-16941508-AGATGACACGTCAAGAAGAGCGAGTCCCACTTC-A
• gnomAD v4: 17-16941508-AGATGACACGTCAAGAAGAGCGAGTCCCACTTC-A
• MyVariant Identifiers: chr17:g.16844823_16844854del (hg19) ; chr17:g.16941509_16941540del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16941510_16941541del , CM000679.2:g.16941510_16941541del	GRCh38
NC_000017.10:g.16844824_16844855del , CM000679.1:g.16844824_16844855del	GRCh37
NC_000017.9:g.16785549_16785580del	NCBI36
NG_007281.1:g.35549_35580del , LRG_120:g.35549_35580del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.446-1029_446-998del MANE Select	ENSP00000261652.2:n.446-1029_446-998del
ENST00000261652.6:c.446-1029_446-998del	ENSP00000261652.2:n.446-1029_446-998del
ENST00000579315.5:c.445+7198_445+7229del	ENSP00000464069.1:n.445+7198_445+7229del
ENST00000581616.2:n.449-63_449-32del
ENST00000582931.5:n.349+7198_349+7229del
ENST00000583789.1:c.308-1029_308-998del	ENSP00000462952.1:n.308-1029_308-998del
ENST00000584950.5:c.308-1029_308-998del	ENSP00000463582.1:n.308-1029_308-998del
NM_012452.2:c.446-1029_446-998del , LRG_120t1:c.446-1029_446-998del	NP_036584.1:n.446-1029_446-998del
NM_012452.3:c.446-1029_446-998del MANE Select	NP_036584.1:n.446-1029_446-998del