Canonical Allele Identifier: CA717052680

Gene: VPS33B

Linked Data

• dbSNP Id: rs377488699
• gnomAD v4: 15-91022271-G-C
• MyVariant Identifiers: chr15:g.91565501G>C (hg19) ; chr15:g.91022271G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022271G>C , CM000677.2:g.91022271G>C	GRCh38
NC_000015.9:g.91565501G>C , CM000677.1:g.91565501G>C	GRCh37
NC_000015.8:g.89366505G>C	NCBI36
NG_012162.1:g.5333C>G , LRG_884:g.5333C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-22C>G MANE Select	ENSP00000327650.4:n.-22C>G
ENST00000643536.1:c.-22C>G	ENSP00000494429.1:n.-22C>G
ENST00000647331.1:c.-22C>G	ENSP00000493953.1:n.-22C>G
ENST00000333371.7:c.-22C>G	ENSP00000327650.3:n.-22C>G
ENST00000535906.1:c.-22C>G	ENSP00000444053.1:n.-22C>G
ENST00000556096.6:n.333C>G
ENST00000557358.1:n.326C>G
ENST00000574755.5:c.-22C>G	ENSP00000460413.1:n.-22C>G
NM_001289148.1:c.-22C>G	NP_001276077.1:n.-22C>G
NM_001289149.1:c.-233C>G	NP_001276078.1:n.-233C>G
NM_018668.4:c.-22C>G , LRG_884t1:c.-22C>G	NP_061138.3:n.-22C>G
XM_005254884.2:c.-22C>G	XP_005254941.1:n.-22C>G
XM_005254887.1:c.-152C>G	XP_005254944.1:n.-152C>G
XM_005254888.2:c.-22C>G	XP_005254945.1:n.-22C>G
XM_011521448.1:c.-335C>G	XP_011519750.1:n.-335C>G
XM_017022075.2:c.-383C>G	XP_016877564.1:n.-383C>G
XM_017022076.1:c.-240C>G	XP_016877565.1:n.-240C>G
XR_001751213.2:n.315C>G
NM_018668.5:c.-22C>G MANE Select	NP_061138.3:n.-22C>G