Canonical Allele Identifier: CA2636329192
Gene: TNFRSF13B HGNC NCBI

Linked Data

gnomAD v4: 17-16948657-TCCTGTTCTAGG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16948662_16948672del , CM000679.2:g.16948662_16948672del GRCh38
NC_000017.10:g.16851976_16851986del , CM000679.1:g.16851976_16851986del GRCh37
NC_000017.9:g.16792701_16792711del NCBI36
NG_007281.1:g.28421_28431del , LRG_120:g.28421_28431del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.445+70_445+80del MANE Select ENSP00000261652.2:n.445+70_445+80del
ENST00000261652.6:c.445+70_445+80del ENSP00000261652.2:n.445+70_445+80del
ENST00000579315.5:c.445+70_445+80del ENSP00000464069.1:n.445+70_445+80del
ENST00000581616.2:n.448+70_448+80del
ENST00000582931.5:n.349+70_349+80del
ENST00000583789.1:c.307+70_307+80del ENSP00000462952.1:n.307+70_307+80del
ENST00000584950.5:c.307+70_307+80del ENSP00000463582.1:n.307+70_307+80del
NM_012452.2:c.445+70_445+80del , LRG_120t1:c.445+70_445+80del NP_036584.1:n.445+70_445+80del
NM_012452.3:c.445+70_445+80del MANE Select NP_036584.1:n.445+70_445+80del
Search 100 bp 5'
Search 100 bp 3'