Canonical Allele Identifier: CA2630423976

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022445-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022445A>G , CM000677.2:g.91022445A>G	GRCh38
NC_000015.9:g.91565675A>G , CM000677.1:g.91565675A>G	GRCh37
NC_000015.8:g.89366679A>G	NCBI36
NG_012162.1:g.5159T>C , LRG_884:g.5159T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-196T>C MANE Select	ENSP00000327650.4:n.-196T>C
ENST00000643536.1:c.-196T>C	ENSP00000494429.1:n.-196T>C
ENST00000333371.7:c.-196T>C	ENSP00000327650.3:n.-196T>C
ENST00000535906.1:c.-196T>C	ENSP00000444053.1:n.-196T>C
ENST00000556096.6:n.159T>C
ENST00000557358.1:n.152T>C
ENST00000574755.5:c.-196T>C	ENSP00000460413.1:n.-196T>C
NM_001289148.1:c.-196T>C	NP_001276077.1:n.-196T>C
NM_001289149.1:c.-407T>C	NP_001276078.1:n.-407T>C
NM_018668.4:c.-196T>C , LRG_884t1:c.-196T>C	NP_061138.3:n.-196T>C
XM_005254884.2:c.-196T>C	XP_005254941.1:n.-196T>C
XM_005254887.1:c.-326T>C	XP_005254944.1:n.-326T>C
XM_005254888.2:c.-196T>C	XP_005254945.1:n.-196T>C
XM_011521448.1:c.-509T>C	XP_011519750.1:n.-509T>C
XM_017022075.2:c.-557T>C	XP_016877564.1:n.-557T>C
XM_017022076.1:c.-414T>C	XP_016877565.1:n.-414T>C
XR_001751213.2:n.141T>C
NM_018668.5:c.-196T>C MANE Select	NP_061138.3:n.-196T>C