Canonical Allele Identifier: CA717052841

Gene: VPS33B

Linked Data

• dbSNP Id: rs1242435067
• gnomAD v4: 15-91022588-C-A
• MyVariant Identifiers: chr15:g.91565818C>A (hg19) ; chr15:g.91022588C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.91022588C>A , CM000677.2:g.91022588C>A	GRCh38
NC_000015.9:g.91565818C>A , CM000677.1:g.91565818C>A	GRCh37
NC_000015.8:g.89366822C>A	NCBI36
NG_012162.1:g.5016G>T , LRG_884:g.5016G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333371.8:c.-339G>T MANE Select	ENSP00000327650.4:n.-339G>T
ENST00000333371.7:c.-339G>T	ENSP00000327650.3:n.-339G>T
ENST00000535906.1:c.-339G>T	ENSP00000444053.1:n.-339G>T
ENST00000556096.6:n.16G>T
ENST00000557358.1:n.9G>T
NM_001289148.1:c.-339G>T	NP_001276077.1:n.-339G>T
NM_001289149.1:c.-550G>T	NP_001276078.1:n.-550G>T
NM_018668.4:c.-339G>T , LRG_884t1:c.-339G>T	NP_061138.3:n.-339G>T
XM_005254887.1:c.-469G>T	XP_005254944.1:n.-469G>T
XM_011521448.1:c.-652G>T	XP_011519750.1:n.-652G>T
XM_017022075.2:c.-700G>T	XP_016877564.1:n.-700G>T
XM_017022076.1:c.-557G>T	XP_016877565.1:n.-557G>T
NM_018668.5:c.-339G>T MANE Select	NP_061138.3:n.-339G>T