Canonical Allele Identifier: CA422814682
Gene: KIF21B HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.200960212C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.200991084C>T , CM000663.2:g.200991084C>T GRCh38
NC_000001.10:g.200960212C>T , CM000663.1:g.200960212C>T GRCh37
NC_000001.9:g.199226835C>T NCBI36
NG_047130.1:g.37617G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000461742.7:c.2520G>A MANE Select ENSP00000433808.1:p.Lys840=
ENST00000332129.6:c.2520G>A ENSP00000328494.2:p.Lys840=
ENST00000360529.9:c.2520G>A ENSP00000353724.5:p.Lys840=
ENST00000422435.2:c.2520G>A ENSP00000411831.2:p.Lys840=
ENST00000461742.6:c.2520G>A ENSP00000433808.1:p.Lys840=
NM_001252100.1:c.2520G>A NP_001239029.1:p.Lys840=
NM_001252102.1:c.2520G>A NP_001239031.1:p.Lys840=
NM_001252103.1:c.2520G>A NP_001239032.1:p.Lys840=
NM_017596.3:c.2520G>A NP_060066.2:p.Lys840=
XR_921754.1:n.2626G>A
XR_921755.1:n.2459G>A
XR_921756.1:n.1594G>A
XR_921757.1:n.1621G>A
XR_921758.1:n.953G>A
XM_017000731.1:c.2352G>A XP_016856220.1:p.Lys784=
XM_017000732.1:c.1317G>A XP_016856221.1:p.Lys439=
NM_001252100.2:c.2520G>A NP_001239029.1:p.Lys840=
NM_001252102.2:c.2520G>A MANE Select NP_001239031.1:p.Lys840=
NM_001252103.2:c.2520G>A NP_001239032.1:p.Lys840=
NM_017596.4:c.2520G>A NP_060066.2:p.Lys840=