Canonical Allele Identifier: CA726572799
Gene: TNFRSF13B HGNC NCBI

Linked Data

dbSNP Id: rs1318666883
gnomAD v3: 17-16941543-GC-G
gnomAD v4: 17-16941543-GC-G
MyVariant Identifiers: chr17:g.16844858del (hg19) chr17:g.16941544del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16941545del , CM000679.2:g.16941545del GRCh38
NC_000017.10:g.16844859del , CM000679.1:g.16844859del GRCh37
NC_000017.9:g.16785584del NCBI36
NG_007281.1:g.35545del , LRG_120:g.35545del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.446-1033del MANE Select ENSP00000261652.2:n.446-1033del
ENST00000261652.6:c.446-1033del ENSP00000261652.2:n.446-1033del
ENST00000579315.5:c.445+7194del ENSP00000464069.1:n.445+7194del
ENST00000581616.2:n.449-67del
ENST00000582931.5:n.349+7194del
ENST00000583789.1:c.308-1033del ENSP00000462952.1:n.308-1033del
ENST00000584950.5:c.308-1033del ENSP00000463582.1:n.308-1033del
NM_012452.2:c.446-1033del , LRG_120t1:c.446-1033del NP_036584.1:n.446-1033del
NM_012452.3:c.446-1033del MANE Select NP_036584.1:n.446-1033del
Search 100 bp 5'
Search 100 bp 3'