Canonical Allele Identifier: CA2630424706

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022577-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022577A>T , CM000677.2:g.91022577A>T	GRCh38
NC_000015.9:g.91565807A>T , CM000677.1:g.91565807A>T	GRCh37
NC_000015.8:g.89366811A>T	NCBI36
NG_012162.1:g.5027T>A , LRG_884:g.5027T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-328T>A MANE Select	ENSP00000327650.4:n.-328T>A
ENST00000333371.7:c.-328T>A	ENSP00000327650.3:n.-328T>A
ENST00000535906.1:c.-328T>A	ENSP00000444053.1:n.-328T>A
ENST00000556096.6:n.27T>A
ENST00000557358.1:n.20T>A
NM_001289148.1:c.-328T>A	NP_001276077.1:n.-328T>A
NM_001289149.1:c.-539T>A	NP_001276078.1:n.-539T>A
NM_018668.4:c.-328T>A , LRG_884t1:c.-328T>A	NP_061138.3:n.-328T>A
XM_005254884.2:c.-328T>A	XP_005254941.1:n.-328T>A
XM_005254887.1:c.-458T>A	XP_005254944.1:n.-458T>A
XM_005254888.2:c.-328T>A	XP_005254945.1:n.-328T>A
XM_011521448.1:c.-641T>A	XP_011519750.1:n.-641T>A
XM_017022075.2:c.-689T>A	XP_016877564.1:n.-689T>A
XM_017022076.1:c.-546T>A	XP_016877565.1:n.-546T>A
XR_001751213.2:n.9T>A
NM_018668.5:c.-328T>A MANE Select	NP_061138.3:n.-328T>A