Canonical Allele Identifier: CA972735248

Gene: VPS33B

Linked Data

• dbSNP Id: rs2041128188
• gnomAD v3: 15-91022287-C-T
• gnomAD v4: 15-91022287-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022287C>T , CM000677.2:g.91022287C>T	GRCh38
NC_000015.9:g.91565517C>T , CM000677.1:g.91565517C>T	GRCh37
NC_000015.8:g.89366521C>T	NCBI36
NG_012162.1:g.5317G>A , LRG_884:g.5317G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-38G>A MANE Select	ENSP00000327650.4:n.-38G>A
ENST00000643536.1:c.-38G>A	ENSP00000494429.1:n.-38G>A
ENST00000647331.1:c.-38G>A	ENSP00000493953.1:n.-38G>A
ENST00000333371.7:c.-38G>A	ENSP00000327650.3:n.-38G>A
ENST00000535906.1:c.-38G>A	ENSP00000444053.1:n.-38G>A
ENST00000556096.6:n.317G>A
ENST00000557358.1:n.310G>A
ENST00000574755.5:c.-38G>A	ENSP00000460413.1:n.-38G>A
NM_001289148.1:c.-38G>A	NP_001276077.1:n.-38G>A
NM_001289149.1:c.-249G>A	NP_001276078.1:n.-249G>A
NM_018668.4:c.-38G>A , LRG_884t1:c.-38G>A	NP_061138.3:n.-38G>A
XM_005254884.2:c.-38G>A	XP_005254941.1:n.-38G>A
XM_005254887.1:c.-168G>A	XP_005254944.1:n.-168G>A
XM_005254888.2:c.-38G>A	XP_005254945.1:n.-38G>A
XM_011521448.1:c.-351G>A	XP_011519750.1:n.-351G>A
XM_017022075.2:c.-399G>A	XP_016877564.1:n.-399G>A
XM_017022076.1:c.-256G>A	XP_016877565.1:n.-256G>A
XR_001751213.2:n.299G>A
NM_018668.5:c.-38G>A MANE Select	NP_061138.3:n.-38G>A