Canonical Allele Identifier: CA619588529

Gene: VPS33B

Linked Data

• dbSNP Id: rs1357792463
• gnomAD v2: 15-91565807-A-C
• gnomAD v4: 15-91022577-A-C
• MyVariant Identifiers: chr15:g.91565807A>C (hg19) ; chr15:g.91022577A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022577A>C , CM000677.2:g.91022577A>C	GRCh38
NC_000015.9:g.91565807A>C , CM000677.1:g.91565807A>C	GRCh37
NC_000015.8:g.89366811A>C	NCBI36
NG_012162.1:g.5027T>G , LRG_884:g.5027T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000333371.8:c.-328T>G MANE Select	ENSP00000327650.4:n.-328T>G
ENST00000333371.7:c.-328T>G	ENSP00000327650.3:n.-328T>G
ENST00000535906.1:c.-328T>G	ENSP00000444053.1:n.-328T>G
ENST00000556096.6:n.27T>G
ENST00000557358.1:n.20T>G
NM_001289148.1:c.-328T>G	NP_001276077.1:n.-328T>G
NM_001289149.1:c.-539T>G	NP_001276078.1:n.-539T>G
NM_018668.4:c.-328T>G , LRG_884t1:c.-328T>G	NP_061138.3:n.-328T>G
XM_005254884.2:c.-328T>G	XP_005254941.1:n.-328T>G
XM_005254887.1:c.-458T>G	XP_005254944.1:n.-458T>G
XM_005254888.2:c.-328T>G	XP_005254945.1:n.-328T>G
XM_011521448.1:c.-641T>G	XP_011519750.1:n.-641T>G
XM_017022075.2:c.-689T>G	XP_016877564.1:n.-689T>G
XM_017022076.1:c.-546T>G	XP_016877565.1:n.-546T>G
XR_001751213.2:n.9T>G
NM_018668.5:c.-328T>G MANE Select	NP_061138.3:n.-328T>G