Canonical Allele Identifier: CA272775
Gene: WDR62 HGNC NCBI

Linked Data

ClinVar Variation Id: 160272
ClinVar RCV Id: RCV000147941
dbSNP Id: rs587784549
MyVariant Identifiers: chr19:g.36590435C>G (hg19) chr19:g.36099533C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36099533C>G , CM000681.2:g.36099533C>G GRCh38
NC_000019.9:g.36590435C>G , CM000681.1:g.36590435C>G GRCh37
NC_000019.8:g.41282275C>G NCBI36
NG_028101.1:g.49653C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000270301.12:c.2655C>G ENSP00000270301.6:p.Tyr885Ter
ENST00000401500.7:c.2655C>G MANE Select ENSP00000384792.1:p.Tyr885Ter
ENST00000587391.6:c.*1345C>G ENSP00000465525.1:n.*1345C>G
ENST00000679357.1:c.445C>G
ENST00000679422.1:c.445C>G
ENST00000679682.1:c.2640C>G ENSP00000506226.1:p.Tyr880Ter
ENST00000679714.1:c.2649C>G ENSP00000506627.1:p.Tyr883Ter
ENST00000679757.1:c.2304C>G ENSP00000505158.1:p.Tyr768Ter
ENST00000679858.1:c.*1452C>G ENSP00000505655.1:n.*1452C>G
ENST00000680349.1:n.638C>G
ENST00000680377.1:c.929C>G
ENST00000680403.1:c.2655C>G ENSP00000505677.1:p.Tyr885Ter
ENST00000680564.1:c.2655C>G ENSP00000505582.1:p.Tyr885Ter
ENST00000680590.1:c.*1054C>G ENSP00000505350.1:n.*1054C>G
ENST00000680806.1:c.*1484C>G ENSP00000506418.1:n.*1484C>G
ENST00000680858.1:c.853C>G
ENST00000681088.1:c.445C>G
ENST00000681302.1:c.1041C>G
ENST00000681625.1:c.2636C>G ENSP00000505555.1:p.Thr879Ser
ENST00000270301.11:c.2655C>G ENSP00000270301.6:p.Tyr885Ter
ENST00000401500.6:c.2655C>G ENSP00000384792.1:p.Tyr885Ter
ENST00000587391.5:c.*1345C>G ENSP00000465525.1:n.*1345C>G
NM_001083961.1:c.2655C>G NP_001077430.1:p.Tyr885Ter
NM_173636.4:c.2655C>G NP_775907.4:p.Tyr885Ter
XM_005258809.2:c.2655C>G XP_005258866.1:p.Tyr885Ter
XM_011526837.1:c.2640C>G XP_011525139.1:p.Tyr880Ter
XM_011526838.1:c.2655C>G XP_011525140.1:p.Tyr885Ter
XM_011526839.1:c.2304C>G XP_011525141.1:p.Tyr768Ter
XM_011526840.1:c.1647C>G XP_011525142.1:p.Tyr549Ter
XM_011526841.1:c.1233C>G XP_011525143.1:p.Tyr411Ter
XM_011526842.1:c.1086C>G XP_011525144.1:p.Tyr362Ter
XM_011526843.1:c.402C>G XP_011525145.1:p.Tyr134Ter
XM_011526844.1:c.402C>G XP_011525146.1:p.Tyr134Ter
XM_011526840.2:c.1647C>G XP_011525142.1:p.Tyr549Ter
XM_011526841.2:c.1233C>G XP_011525143.1:p.Tyr411Ter
XM_011526844.2:c.402C>G XP_011525146.1:p.Tyr134Ter
XM_017026665.1:c.2655C>G XP_016882154.1:p.Tyr885Ter
NM_001083961.2:c.2655C>G MANE Select NP_001077430.1:p.Tyr885Ter
NM_173636.5:c.2655C>G NP_775907.4:p.Tyr885Ter
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