Canonical Allele Identifier: CA2636331528

Gene: TNFRSF13B

Linked Data

• gnomAD v4: 17-16941523-A-AAGAGCGAGTCCCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16941524_16941537dup , CM000679.2:g.16941524_16941537dup	GRCh38
NC_000017.10:g.16844838_16844851dup , CM000679.1:g.16844838_16844851dup	GRCh37
NC_000017.9:g.16785563_16785576dup	NCBI36
NG_007281.1:g.35552_35565dup , LRG_120:g.35552_35565dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261652.7:c.446-1026_446-1013dup MANE Select	ENSP00000261652.2:n.446-1026_446-1013dup
ENST00000261652.6:c.446-1026_446-1013dup	ENSP00000261652.2:n.446-1026_446-1013dup
ENST00000579315.5:c.445+7201_445+7214dup	ENSP00000464069.1:n.445+7201_445+7214dup
ENST00000581616.2:n.449-60_449-47dup
ENST00000582931.5:n.349+7201_349+7214dup
ENST00000583789.1:c.308-1026_308-1013dup	ENSP00000462952.1:n.308-1026_308-1013dup
ENST00000584950.5:c.308-1026_308-1013dup	ENSP00000463582.1:n.308-1026_308-1013dup
NM_012452.2:c.446-1026_446-1013dup , LRG_120t1:c.446-1026_446-1013dup	NP_036584.1:n.446-1026_446-1013dup
NM_012452.3:c.446-1026_446-1013dup MANE Select	NP_036584.1:n.446-1026_446-1013dup