Canonical Allele Identifier: CA405450655
Gene: WDR62 HGNC NCBI

Linked Data

dbSNP Id: rs1392806686

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102115C>T , CM000681.2:g.36102115C>T GRCh38
NC_000019.9:g.36593017C>T , CM000681.1:g.36593017C>T GRCh37
NC_000019.8:g.41284857C>T NCBI36
NG_028101.1:g.52235C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3184C>T ENSP00000270301.6:p.His1062Tyr
ENST00000401500.7:c.3184C>T MANE Select ENSP00000384792.1:p.His1062Tyr
ENST00000587391.6:c.*2459C>T ENSP00000465525.1:n.*2459C>T
ENST00000679357.1:c.974C>T
ENST00000679422.1:c.863C>T
ENST00000679682.1:c.3169C>T ENSP00000506226.1:p.His1057Tyr
ENST00000679714.1:c.3178C>T ENSP00000506627.1:p.His1060Tyr
ENST00000679757.1:c.2833C>T ENSP00000505158.1:p.His945Tyr
ENST00000679858.1:c.*2566C>T ENSP00000505655.1:n.*2566C>T
ENST00000680211.1:c.-216C>T ENSP00000506102.1:n.-216C>T
ENST00000680349.1:n.1167C>T
ENST00000680403.1:c.3184C>T ENSP00000505677.1:p.His1062Tyr
ENST00000680564.1:c.2972-622C>T ENSP00000505582.1:n.2972-622C>T
ENST00000680590.1:c.*1579C>T ENSP00000505350.1:n.*1579C>T
ENST00000680739.1:c.102C>T
ENST00000680773.1:n.1100C>T
ENST00000680806.1:c.*1902C>T ENSP00000506418.1:n.*1902C>T
ENST00000680997.1:n.531C>T
ENST00000681088.1:c.846C>T
ENST00000681608.1:n.132C>T
ENST00000681625.1:c.*516C>T ENSP00000505555.1:n.*516C>T
ENST00000270301.11:c.3184C>T ENSP00000270301.6:p.His1062Tyr
ENST00000401500.6:c.3184C>T ENSP00000384792.1:p.His1062Tyr
ENST00000587391.5:c.*2459C>T ENSP00000465525.1:n.*2459C>T
NM_001083961.1:c.3184C>T NP_001077430.1:p.His1062Tyr
NM_173636.4:c.3184C>T NP_775907.4:p.His1062Tyr
XM_005258809.2:c.3073C>T XP_005258866.1:p.His1025Tyr
XM_011526837.1:c.3169C>T XP_011525139.1:p.His1057Tyr
XM_011526838.1:c.2972-622C>T XP_011525140.1:n.2972-622C>T
XM_011526839.1:c.2833C>T XP_011525141.1:p.His945Tyr
XM_011526840.1:c.2176C>T XP_011525142.1:p.His726Tyr
XM_011526841.1:c.1762C>T XP_011525143.1:p.His588Tyr
XM_011526842.1:c.1615C>T XP_011525144.1:p.His539Tyr
XM_011526843.1:c.931C>T XP_011525145.1:p.His311Tyr
XM_011526844.1:c.931C>T XP_011525146.1:p.His311Tyr
XM_011526840.2:c.2176C>T XP_011525142.1:p.His726Tyr
XM_011526841.2:c.1762C>T XP_011525143.1:p.His588Tyr
XM_011526844.2:c.931C>T XP_011525146.1:p.His311Tyr
XM_017026665.1:c.3184C>T XP_016882154.1:p.His1062Tyr
NM_001083961.2:c.3184C>T MANE Select NP_001077430.1:p.His1062Tyr
NM_173636.5:c.3184C>T NP_775907.4:p.His1062Tyr