Canonical Allele Identifier: CA2630423198

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022283-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022283C>G , CM000677.2:g.91022283C>G	GRCh38
NC_000015.9:g.91565513C>G , CM000677.1:g.91565513C>G	GRCh37
NC_000015.8:g.89366517C>G	NCBI36
NG_012162.1:g.5321G>C , LRG_884:g.5321G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-34G>C MANE Select	ENSP00000327650.4:n.-34G>C
ENST00000643536.1:c.-34G>C	ENSP00000494429.1:n.-34G>C
ENST00000647331.1:c.-34G>C	ENSP00000493953.1:n.-34G>C
ENST00000333371.7:c.-34G>C	ENSP00000327650.3:n.-34G>C
ENST00000535906.1:c.-34G>C	ENSP00000444053.1:n.-34G>C
ENST00000556096.6:n.321G>C
ENST00000557358.1:n.314G>C
ENST00000574755.5:c.-34G>C	ENSP00000460413.1:n.-34G>C
NM_001289148.1:c.-34G>C	NP_001276077.1:n.-34G>C
NM_001289149.1:c.-245G>C	NP_001276078.1:n.-245G>C
NM_018668.4:c.-34G>C , LRG_884t1:c.-34G>C	NP_061138.3:n.-34G>C
XM_005254884.2:c.-34G>C	XP_005254941.1:n.-34G>C
XM_005254887.1:c.-164G>C	XP_005254944.1:n.-164G>C
XM_005254888.2:c.-34G>C	XP_005254945.1:n.-34G>C
XM_011521448.1:c.-347G>C	XP_011519750.1:n.-347G>C
XM_017022075.2:c.-395G>C	XP_016877564.1:n.-395G>C
XM_017022076.1:c.-252G>C	XP_016877565.1:n.-252G>C
XR_001751213.2:n.303G>C
NM_018668.5:c.-34G>C MANE Select	NP_061138.3:n.-34G>C