Canonical Allele Identifier: CA2630424756

Gene: VPS33B

Linked Data

• gnomAD v4: 15-91022591-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022591C>A , CM000677.2:g.91022591C>A	GRCh38
NC_000015.9:g.91565821C>A , CM000677.1:g.91565821C>A	GRCh37
NC_000015.8:g.89366825C>A	NCBI36
NG_012162.1:g.5013G>T , LRG_884:g.5013G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-342G>T MANE Select	ENSP00000327650.4:n.-342G>T
ENST00000333371.7:c.-342G>T	ENSP00000327650.3:n.-342G>T
ENST00000535906.1:c.-342G>T	ENSP00000444053.1:n.-342G>T
ENST00000556096.6:n.13G>T
ENST00000557358.1:n.6G>T
NM_001289148.1:c.-342G>T	NP_001276077.1:n.-342G>T
NM_001289149.1:c.-553G>T	NP_001276078.1:n.-553G>T
NM_018668.4:c.-342G>T , LRG_884t1:c.-342G>T	NP_061138.3:n.-342G>T
XM_005254887.1:c.-472G>T	XP_005254944.1:n.-472G>T
XM_011521448.1:c.-655G>T	XP_011519750.1:n.-655G>T
XM_017022075.2:c.-703G>T	XP_016877564.1:n.-703G>T
XM_017022076.1:c.-560G>T	XP_016877565.1:n.-560G>T
NM_018668.5:c.-342G>T MANE Select	NP_061138.3:n.-342G>T