Canonical Allele Identifier: CA1231304244
Gene: KIF26B HGNC NCBI

Linked Data

dbSNP Id: rs954941550

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.245570340T>C , CM000663.2:g.245570340T>C GRCh38
NC_000001.10:g.245733642T>C , CM000663.1:g.245733642T>C GRCh37
NC_000001.9:g.243800265T>C NCBI36
NG_053061.1:g.420356T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000407071.7:c.1350+29390T>C MANE Select ENSP00000385545.2:n.1350+29390T>C
ENST00000366518.4:c.207+29390T>C ENSP00000355475.4:n.207+29390T>C
ENST00000407071.6:c.1350+29390T>C ENSP00000385545.2:n.1350+29390T>C
NM_018012.3:c.1350+29390T>C NP_060482.2:n.1350+29390T>C
XM_011544214.1:c.912+29390T>C XP_011542516.1:n.912+29390T>C
XM_011544215.1:c.750+29390T>C XP_011542517.1:n.750+29390T>C
XM_011544216.1:c.750+29390T>C XP_011542518.1:n.750+29390T>C
XM_011544217.1:c.750+29390T>C XP_011542519.1:n.750+29390T>C
XM_011544218.1:c.207+29390T>C XP_011542520.1:n.207+29390T>C
NM_018012.4:c.1350+29390T>C MANE Select NP_060482.2:n.1350+29390T>C