Canonical Allele Identifier: CA2195408469

Gene: VPS33B

Linked Data

• dbSNP Id: rs1596376210
• gnomAD v4: 15-91022438-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022438A>C , CM000677.2:g.91022438A>C	GRCh38
NC_000015.9:g.91565668A>C , CM000677.1:g.91565668A>C	GRCh37
NC_000015.8:g.89366672A>C	NCBI36
NG_012162.1:g.5166T>G , LRG_884:g.5166T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-189T>G MANE Select	ENSP00000327650.4:n.-189T>G
ENST00000643536.1:c.-189T>G	ENSP00000494429.1:n.-189T>G
ENST00000333371.7:c.-189T>G	ENSP00000327650.3:n.-189T>G
ENST00000535906.1:c.-189T>G	ENSP00000444053.1:n.-189T>G
ENST00000556096.6:n.166T>G
ENST00000557358.1:n.159T>G
ENST00000574755.5:c.-189T>G	ENSP00000460413.1:n.-189T>G
NM_001289148.1:c.-189T>G	NP_001276077.1:n.-189T>G
NM_001289149.1:c.-400T>G	NP_001276078.1:n.-400T>G
NM_018668.4:c.-189T>G , LRG_884t1:c.-189T>G	NP_061138.3:n.-189T>G
XM_005254884.2:c.-189T>G	XP_005254941.1:n.-189T>G
XM_005254887.1:c.-319T>G	XP_005254944.1:n.-319T>G
XM_005254888.2:c.-189T>G	XP_005254945.1:n.-189T>G
XM_011521448.1:c.-502T>G	XP_011519750.1:n.-502T>G
XM_017022075.2:c.-550T>G	XP_016877564.1:n.-550T>G
XM_017022076.1:c.-407T>G	XP_016877565.1:n.-407T>G
XR_001751213.2:n.148T>G
NM_018668.5:c.-189T>G MANE Select	NP_061138.3:n.-189T>G