Canonical Allele Identifier: CA857579972

Gene: VPS13B

Linked Data

• dbSNP Id: rs1350456791
• MyVariant Identifiers: chr8:g.100711652T>C (hg19) ; chr8:g.99699424T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.99699424T>C , CM000670.2:g.99699424T>C	GRCh38
NC_000008.10:g.100711652T>C , CM000670.1:g.100711652T>C	GRCh37
NC_000008.9:g.100780828T>C	NCBI36
NG_007098.2:g.691159T>C , LRG_351:g.691159T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682153.1:c.6122-101T>C	ENSP00000507923.1:n.6122-101T>C
ENST00000682358.1:n.6192-101T>C
ENST00000683334.1:c.*1804-101T>C	ENSP00000507369.1:n.*1804-101T>C
ENST00000357162.7:c.6047-101T>C MANE Select	ENSP00000349685.2:n.6047-101T>C
ENST00000358544.7:c.6122-101T>C MANE Plus Clinical	ENSP00000351346.2:n.6122-101T>C
ENST00000357162.6:c.6047-101T>C	ENSP00000349685.2:n.6047-101T>C
ENST00000358544.6:c.6122-101T>C	ENSP00000351346.2:n.6122-101T>C
NM_017890.4:c.6122-101T>C , LRG_351t1:c.6122-101T>C	NP_060360.3:n.6122-101T>C
NM_152564.4:c.6047-101T>C , LRG_351t2:c.6047-101T>C	NP_689777.3:n.6047-101T>C
XM_005250800.2:c.6122-101T>C	XP_005250857.1:n.6122-101T>C
XM_005250801.3:c.6122-101T>C	XP_005250858.1:n.6122-101T>C
XM_011516848.1:c.6119-101T>C	XP_011515150.1:n.6119-101T>C
XM_011516849.1:c.6044-101T>C	XP_011515151.1:n.6044-101T>C
XM_011516850.1:c.5744-101T>C	XP_011515152.1:n.5744-101T>C
XM_011516851.1:c.3008-101T>C	XP_011515153.1:n.3008-101T>C
XM_011516852.1:c.3008-101T>C	XP_011515154.1:n.3008-101T>C
XM_011516853.1:c.6122-101T>C	XP_011515155.1:n.6122-101T>C
XM_011516854.1:c.1901-101T>C	XP_011515156.1:n.1901-101T>C
XM_005250800.3:c.6122-101T>C	XP_005250857.1:n.6122-101T>C
XM_005250801.5:c.6122-101T>C	XP_005250858.1:n.6122-101T>C
XM_011516848.2:c.6119-101T>C	XP_011515150.1:n.6119-101T>C
XM_011516849.2:c.6044-101T>C	XP_011515151.1:n.6044-101T>C
XM_011516850.2:c.5744-101T>C	XP_011515152.1:n.5744-101T>C
XM_011516851.2:c.3008-101T>C	XP_011515153.1:n.3008-101T>C
XM_011516852.2:c.3008-101T>C	XP_011515154.1:n.3008-101T>C
XM_011516853.2:c.6122-101T>C	XP_011515155.1:n.6122-101T>C
XM_011516854.2:c.1901-101T>C	XP_011515156.1:n.1901-101T>C
XM_017013109.1:c.5927-101T>C	XP_016868598.1:n.5927-101T>C
XM_017013111.1:c.3008-101T>C	XP_016868600.1:n.3008-101T>C
XM_017013112.1:c.1679-101T>C	XP_016868601.1:n.1679-101T>C
XM_024447074.1:c.4907-101T>C	XP_024302842.1:n.4907-101T>C
XR_001745482.2:n.6083-101T>C
NM_017890.5:c.6122-101T>C MANE Plus Clinical	NP_060360.3:n.6122-101T>C
NM_152564.5:c.6047-101T>C MANE Select	NP_689777.3:n.6047-101T>C