Canonical Allele Identifier: CA2636329212

Gene: TNFRSF13B

Linked Data

• gnomAD v4: 17-16948680-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16948682dup , CM000679.2:g.16948682dup	GRCh38
NC_000017.10:g.16851996dup , CM000679.1:g.16851996dup	GRCh37
NC_000017.9:g.16792721dup	NCBI36
NG_007281.1:g.28408dup , LRG_120:g.28408dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000261652.7:c.445+57dup MANE Select	ENSP00000261652.2:n.445+57dup
ENST00000261652.6:c.445+57dup	ENSP00000261652.2:n.445+57dup
ENST00000579315.5:c.445+57dup	ENSP00000464069.1:n.445+57dup
ENST00000581616.2:n.448+57dup
ENST00000582931.5:n.349+57dup
ENST00000583789.1:c.307+57dup	ENSP00000462952.1:n.307+57dup
ENST00000584950.5:c.307+57dup	ENSP00000463582.1:n.307+57dup
NM_012452.2:c.445+57dup , LRG_120t1:c.445+57dup	NP_036584.1:n.445+57dup
NM_012452.3:c.445+57dup MANE Select	NP_036584.1:n.445+57dup