Canonical Allele Identifier: CA2576184067
Gene: TNFRSF13B HGNC NCBI

Linked Data

gnomAD v4: 17-16941522-GA-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16941524del , CM000679.2:g.16941524del GRCh38
NC_000017.10:g.16844838del , CM000679.1:g.16844838del GRCh37
NC_000017.9:g.16785563del NCBI36
NG_007281.1:g.35566del , LRG_120:g.35566del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261652.7:c.446-1012del MANE Select ENSP00000261652.2:n.446-1012del
ENST00000261652.6:c.446-1012del ENSP00000261652.2:n.446-1012del
ENST00000579315.5:c.445+7215del ENSP00000464069.1:n.445+7215del
ENST00000581616.2:n.449-46del
ENST00000582931.5:n.349+7215del
ENST00000583789.1:c.308-1012del ENSP00000462952.1:n.308-1012del
ENST00000584950.5:c.308-1012del ENSP00000463582.1:n.308-1012del
NM_012452.2:c.446-1012del , LRG_120t1:c.446-1012del NP_036584.1:n.446-1012del
NM_012452.3:c.446-1012del MANE Select NP_036584.1:n.446-1012del
Search 100 bp 5'
Search 100 bp 3'