Canonical Allele Identifier: CA2195408496

Gene: VPS33B

Linked Data

• dbSNP Id: rs2041134991
• gnomAD v4: 15-91022476-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022476G>T , CM000677.2:g.91022476G>T	GRCh38
NC_000015.9:g.91565706G>T , CM000677.1:g.91565706G>T	GRCh37
NC_000015.8:g.89366710G>T	NCBI36
NG_012162.1:g.5128C>A , LRG_884:g.5128C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-227C>A MANE Select	ENSP00000327650.4:n.-227C>A
ENST00000643536.1:c.-227C>A	ENSP00000494429.1:n.-227C>A
ENST00000333371.7:c.-227C>A	ENSP00000327650.3:n.-227C>A
ENST00000535906.1:c.-227C>A	ENSP00000444053.1:n.-227C>A
ENST00000556096.6:n.128C>A
ENST00000557358.1:n.121C>A
ENST00000574755.5:c.-227C>A	ENSP00000460413.1:n.-227C>A
NM_001289148.1:c.-227C>A	NP_001276077.1:n.-227C>A
NM_001289149.1:c.-438C>A	NP_001276078.1:n.-438C>A
NM_018668.4:c.-227C>A , LRG_884t1:c.-227C>A	NP_061138.3:n.-227C>A
XM_005254884.2:c.-227C>A	XP_005254941.1:n.-227C>A
XM_005254887.1:c.-357C>A	XP_005254944.1:n.-357C>A
XM_005254888.2:c.-227C>A	XP_005254945.1:n.-227C>A
XM_011521448.1:c.-540C>A	XP_011519750.1:n.-540C>A
XM_017022075.2:c.-588C>A	XP_016877564.1:n.-588C>A
XM_017022076.1:c.-445C>A	XP_016877565.1:n.-445C>A
XR_001751213.2:n.110C>A
NM_018668.5:c.-227C>A MANE Select	NP_061138.3:n.-227C>A