Canonical Allele Identifier: CA734015923

Gene: KIF26B

Linked Data

• dbSNP Id: rs1402349315
• gnomAD v3: 1-245570346-T-A
• gnomAD v4: 1-245570346-T-A
• MyVariant Identifiers: chr1:g.245733648T>A (hg19) ; chr1:g.245570346T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.245570346T>A , CM000663.2:g.245570346T>A	GRCh38
NC_000001.10:g.245733648T>A , CM000663.1:g.245733648T>A	GRCh37
NC_000001.9:g.243800271T>A	NCBI36
NG_053061.1:g.420362T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000407071.7:c.1350+29396T>A MANE Select	ENSP00000385545.2:n.1350+29396T>A
ENST00000366518.4:c.207+29396T>A	ENSP00000355475.4:n.207+29396T>A
ENST00000407071.6:c.1350+29396T>A	ENSP00000385545.2:n.1350+29396T>A
NM_018012.3:c.1350+29396T>A	NP_060482.2:n.1350+29396T>A
XM_011544214.1:c.912+29396T>A	XP_011542516.1:n.912+29396T>A
XM_011544215.1:c.750+29396T>A	XP_011542517.1:n.750+29396T>A
XM_011544216.1:c.750+29396T>A	XP_011542518.1:n.750+29396T>A
XM_011544217.1:c.750+29396T>A	XP_011542519.1:n.750+29396T>A
XM_011544218.1:c.207+29396T>A	XP_011542520.1:n.207+29396T>A
NM_018012.4:c.1350+29396T>A MANE Select	NP_060482.2:n.1350+29396T>A