Canonical Allele Identifier: CA2630424741

Gene: VPS33B

Linked Data

• dbSNP Id: rs2151689384
• gnomAD v4: 15-91022586-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022586A>G , CM000677.2:g.91022586A>G	GRCh38
NC_000015.9:g.91565816A>G , CM000677.1:g.91565816A>G	GRCh37
NC_000015.8:g.89366820A>G	NCBI36
NG_012162.1:g.5018T>C , LRG_884:g.5018T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-337T>C MANE Select	ENSP00000327650.4:n.-337T>C
ENST00000333371.7:c.-337T>C	ENSP00000327650.3:n.-337T>C
ENST00000535906.1:c.-337T>C	ENSP00000444053.1:n.-337T>C
ENST00000556096.6:n.18T>C
ENST00000557358.1:n.11T>C
NM_001289148.1:c.-337T>C	NP_001276077.1:n.-337T>C
NM_001289149.1:c.-548T>C	NP_001276078.1:n.-548T>C
NM_018668.4:c.-337T>C , LRG_884t1:c.-337T>C	NP_061138.3:n.-337T>C
XM_005254887.1:c.-467T>C	XP_005254944.1:n.-467T>C
XM_011521448.1:c.-650T>C	XP_011519750.1:n.-650T>C
XM_017022075.2:c.-698T>C	XP_016877564.1:n.-698T>C
XM_017022076.1:c.-555T>C	XP_016877565.1:n.-555T>C
NM_018668.5:c.-337T>C MANE Select	NP_061138.3:n.-337T>C