Canonical Allele Identifier: CA2630424037

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022467-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022467A>G , CM000677.2:g.91022467A>G	GRCh38
NC_000015.9:g.91565697A>G , CM000677.1:g.91565697A>G	GRCh37
NC_000015.8:g.89366701A>G	NCBI36
NG_012162.1:g.5137T>C , LRG_884:g.5137T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-218T>C MANE Select	ENSP00000327650.4:n.-218T>C
ENST00000643536.1:c.-218T>C	ENSP00000494429.1:n.-218T>C
ENST00000333371.7:c.-218T>C	ENSP00000327650.3:n.-218T>C
ENST00000535906.1:c.-218T>C	ENSP00000444053.1:n.-218T>C
ENST00000556096.6:n.137T>C
ENST00000557358.1:n.130T>C
ENST00000574755.5:c.-218T>C	ENSP00000460413.1:n.-218T>C
NM_001289148.1:c.-218T>C	NP_001276077.1:n.-218T>C
NM_001289149.1:c.-429T>C	NP_001276078.1:n.-429T>C
NM_018668.4:c.-218T>C , LRG_884t1:c.-218T>C	NP_061138.3:n.-218T>C
XM_005254884.2:c.-218T>C	XP_005254941.1:n.-218T>C
XM_005254887.1:c.-348T>C	XP_005254944.1:n.-348T>C
XM_005254888.2:c.-218T>C	XP_005254945.1:n.-218T>C
XM_011521448.1:c.-531T>C	XP_011519750.1:n.-531T>C
XM_017022075.2:c.-579T>C	XP_016877564.1:n.-579T>C
XM_017022076.1:c.-436T>C	XP_016877565.1:n.-436T>C
XR_001751213.2:n.119T>C
NM_018668.5:c.-218T>C MANE Select	NP_061138.3:n.-218T>C