Canonical Allele Identifier: CA2630424530

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022537-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022537A>G , CM000677.2:g.91022537A>G	GRCh38
NC_000015.9:g.91565767A>G , CM000677.1:g.91565767A>G	GRCh37
NC_000015.8:g.89366771A>G	NCBI36
NG_012162.1:g.5067T>C , LRG_884:g.5067T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-288T>C MANE Select	ENSP00000327650.4:n.-288T>C
ENST00000643536.1:c.-288T>C	ENSP00000494429.1:n.-288T>C
ENST00000333371.7:c.-288T>C	ENSP00000327650.3:n.-288T>C
ENST00000535906.1:c.-288T>C	ENSP00000444053.1:n.-288T>C
ENST00000556096.6:n.67T>C
ENST00000557358.1:n.60T>C
NM_001289148.1:c.-288T>C	NP_001276077.1:n.-288T>C
NM_001289149.1:c.-499T>C	NP_001276078.1:n.-499T>C
NM_018668.4:c.-288T>C , LRG_884t1:c.-288T>C	NP_061138.3:n.-288T>C
XM_005254884.2:c.-288T>C	XP_005254941.1:n.-288T>C
XM_005254887.1:c.-418T>C	XP_005254944.1:n.-418T>C
XM_005254888.2:c.-288T>C	XP_005254945.1:n.-288T>C
XM_011521448.1:c.-601T>C	XP_011519750.1:n.-601T>C
XM_017022075.2:c.-649T>C	XP_016877564.1:n.-649T>C
XM_017022076.1:c.-506T>C	XP_016877565.1:n.-506T>C
XR_001751213.2:n.49T>C
NM_018668.5:c.-288T>C MANE Select	NP_061138.3:n.-288T>C