Canonical Allele Identifier: CA2630423742

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022402-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022402A>G , CM000677.2:g.91022402A>G	GRCh38
NC_000015.9:g.91565632A>G , CM000677.1:g.91565632A>G	GRCh37
NC_000015.8:g.89366636A>G	NCBI36
NG_012162.1:g.5202T>C , LRG_884:g.5202T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-153T>C MANE Select	ENSP00000327650.4:n.-153T>C
ENST00000643536.1:c.-153T>C	ENSP00000494429.1:n.-153T>C
ENST00000333371.7:c.-153T>C	ENSP00000327650.3:n.-153T>C
ENST00000535906.1:c.-153T>C	ENSP00000444053.1:n.-153T>C
ENST00000556096.6:n.202T>C
ENST00000557358.1:n.195T>C
ENST00000574755.5:c.-153T>C	ENSP00000460413.1:n.-153T>C
NM_001289148.1:c.-153T>C	NP_001276077.1:n.-153T>C
NM_001289149.1:c.-364T>C	NP_001276078.1:n.-364T>C
NM_018668.4:c.-153T>C , LRG_884t1:c.-153T>C	NP_061138.3:n.-153T>C
XM_005254884.2:c.-153T>C	XP_005254941.1:n.-153T>C
XM_005254887.1:c.-283T>C	XP_005254944.1:n.-283T>C
XM_005254888.2:c.-153T>C	XP_005254945.1:n.-153T>C
XM_011521448.1:c.-466T>C	XP_011519750.1:n.-466T>C
XM_017022075.2:c.-514T>C	XP_016877564.1:n.-514T>C
XM_017022076.1:c.-371T>C	XP_016877565.1:n.-371T>C
XR_001751213.2:n.184T>C
NM_018668.5:c.-153T>C MANE Select	NP_061138.3:n.-153T>C