Canonical Allele Identifier: CA2630423972

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022444-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022444G>A , CM000677.2:g.91022444G>A	GRCh38
NC_000015.9:g.91565674G>A , CM000677.1:g.91565674G>A	GRCh37
NC_000015.8:g.89366678G>A	NCBI36
NG_012162.1:g.5160C>T , LRG_884:g.5160C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-195C>T MANE Select	ENSP00000327650.4:n.-195C>T
ENST00000643536.1:c.-195C>T	ENSP00000494429.1:n.-195C>T
ENST00000333371.7:c.-195C>T	ENSP00000327650.3:n.-195C>T
ENST00000535906.1:c.-195C>T	ENSP00000444053.1:n.-195C>T
ENST00000556096.6:n.160C>T
ENST00000557358.1:n.153C>T
ENST00000574755.5:c.-195C>T	ENSP00000460413.1:n.-195C>T
NM_001289148.1:c.-195C>T	NP_001276077.1:n.-195C>T
NM_001289149.1:c.-406C>T	NP_001276078.1:n.-406C>T
NM_018668.4:c.-195C>T , LRG_884t1:c.-195C>T	NP_061138.3:n.-195C>T
XM_005254884.2:c.-195C>T	XP_005254941.1:n.-195C>T
XM_005254887.1:c.-325C>T	XP_005254944.1:n.-325C>T
XM_005254888.2:c.-195C>T	XP_005254945.1:n.-195C>T
XM_011521448.1:c.-508C>T	XP_011519750.1:n.-508C>T
XM_017022075.2:c.-556C>T	XP_016877564.1:n.-556C>T
XM_017022076.1:c.-413C>T	XP_016877565.1:n.-413C>T
XR_001751213.2:n.142C>T
NM_018668.5:c.-195C>T MANE Select	NP_061138.3:n.-195C>T