Canonical Allele Identifier: CA583884518

Gene: VPS13B

Linked Data

• dbSNP Id: rs1432930840
• gnomAD v2: 8-100789217-A-T
• gnomAD v4: 8-99776989-A-T
• MyVariant Identifiers: chr8:g.100789217A>T (hg19) ; chr8:g.99776989A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99776989A>T , CM000670.2:g.99776989A>T	GRCh38
NC_000008.10:g.100789217A>T , CM000670.1:g.100789217A>T	GRCh37
NC_000008.9:g.100858393A>T	NCBI36
NG_007098.2:g.768724A>T , LRG_351:g.768724A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.7504+33A>T	ENSP00000507923.1:n.7504+33A>T
ENST00000682358.1:n.7574+33A>T
ENST00000683334.1:c.*3186+33A>T	ENSP00000507369.1:n.*3186+33A>T
ENST00000357162.7:c.7429+33A>T MANE Select	ENSP00000349685.2:n.7429+33A>T
ENST00000358544.7:c.7504+33A>T MANE Plus Clinical	ENSP00000351346.2:n.7504+33A>T
ENST00000357162.6:c.7429+33A>T	ENSP00000349685.2:n.7429+33A>T
ENST00000358544.6:c.7504+33A>T	ENSP00000351346.2:n.7504+33A>T
ENST00000518569.1:n.378-1693A>T
NM_017890.4:c.7504+33A>T , LRG_351t1:c.7504+33A>T	NP_060360.3:n.7504+33A>T
NM_152564.4:c.7429+33A>T , LRG_351t2:c.7429+33A>T	NP_689777.3:n.7429+33A>T
XM_005250800.2:c.7504+33A>T	XP_005250857.1:n.7504+33A>T
XM_005250801.3:c.7504+33A>T	XP_005250858.1:n.7504+33A>T
XM_011516848.1:c.7501+33A>T	XP_011515150.1:n.7501+33A>T
XM_011516849.1:c.7426+33A>T	XP_011515151.1:n.7426+33A>T
XM_011516850.1:c.7126+33A>T	XP_011515152.1:n.7126+33A>T
XM_011516851.1:c.4390+33A>T	XP_011515153.1:n.4390+33A>T
XM_011516852.1:c.4390+33A>T	XP_011515154.1:n.4390+33A>T
XM_011516853.1:c.7504+33A>T	XP_011515155.1:n.7504+33A>T
XM_011516854.1:c.3283+33A>T	XP_011515156.1:n.3283+33A>T
XR_928446.1:n.1830+5489T>A
XM_005250800.3:c.7504+33A>T	XP_005250857.1:n.7504+33A>T
XM_005250801.5:c.7504+33A>T	XP_005250858.1:n.7504+33A>T
XM_011516848.2:c.7501+33A>T	XP_011515150.1:n.7501+33A>T
XM_011516849.2:c.7426+33A>T	XP_011515151.1:n.7426+33A>T
XM_011516850.2:c.7126+33A>T	XP_011515152.1:n.7126+33A>T
XM_011516851.2:c.4390+33A>T	XP_011515153.1:n.4390+33A>T
XM_011516852.2:c.4390+33A>T	XP_011515154.1:n.4390+33A>T
XM_011516853.2:c.7504+33A>T	XP_011515155.1:n.7504+33A>T
XM_011516854.2:c.3283+33A>T	XP_011515156.1:n.3283+33A>T
XM_017013109.1:c.7309+33A>T	XP_016868598.1:n.7309+33A>T
XM_017013111.1:c.4390+33A>T	XP_016868600.1:n.4390+33A>T
XM_017013112.1:c.3061+33A>T	XP_016868601.1:n.3061+33A>T
XM_024447074.1:c.6289+33A>T	XP_024302842.1:n.6289+33A>T
NM_017890.5:c.7504+33A>T MANE Plus Clinical	NP_060360.3:n.7504+33A>T
NM_152564.5:c.7429+33A>T MANE Select	NP_689777.3:n.7429+33A>T