Canonical Allele Identifier: CA2630423496

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022368-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022368C>A , CM000677.2:g.91022368C>A	GRCh38
NC_000015.9:g.91565598C>A , CM000677.1:g.91565598C>A	GRCh37
NC_000015.8:g.89366602C>A	NCBI36
NG_012162.1:g.5236G>T , LRG_884:g.5236G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-119G>T MANE Select	ENSP00000327650.4:n.-119G>T
ENST00000643536.1:c.-119G>T	ENSP00000494429.1:n.-119G>T
ENST00000333371.7:c.-119G>T	ENSP00000327650.3:n.-119G>T
ENST00000535906.1:c.-119G>T	ENSP00000444053.1:n.-119G>T
ENST00000556096.6:n.236G>T
ENST00000557358.1:n.229G>T
ENST00000574755.5:c.-119G>T	ENSP00000460413.1:n.-119G>T
NM_001289148.1:c.-119G>T	NP_001276077.1:n.-119G>T
NM_001289149.1:c.-330G>T	NP_001276078.1:n.-330G>T
NM_018668.4:c.-119G>T , LRG_884t1:c.-119G>T	NP_061138.3:n.-119G>T
XM_005254884.2:c.-119G>T	XP_005254941.1:n.-119G>T
XM_005254887.1:c.-249G>T	XP_005254944.1:n.-249G>T
XM_005254888.2:c.-119G>T	XP_005254945.1:n.-119G>T
XM_011521448.1:c.-432G>T	XP_011519750.1:n.-432G>T
XM_017022075.2:c.-480G>T	XP_016877564.1:n.-480G>T
XM_017022076.1:c.-337G>T	XP_016877565.1:n.-337G>T
XR_001751213.2:n.218G>T
NM_018668.5:c.-119G>T MANE Select	NP_061138.3:n.-119G>T