Canonical Allele Identifier: CA405450668

Gene: WDR62

Linked Data

• MyVariant Identifiers: chr19:g.36593018A>G (hg19) ; chr19:g.36102116A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102116A>G , CM000681.2:g.36102116A>G	GRCh38
NC_000019.9:g.36593018A>G , CM000681.1:g.36593018A>G	GRCh37
NC_000019.8:g.41284858A>G	NCBI36
NG_028101.1:g.52236A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3185A>G	ENSP00000270301.6:p.His1062Arg
ENST00000401500.7:c.3185A>G MANE Select	ENSP00000384792.1:p.His1062Arg
ENST00000587391.6:c.*2460A>G	ENSP00000465525.1:n.*2460A>G
ENST00000679357.1:c.975A>G
ENST00000679422.1:c.864A>G
ENST00000679682.1:c.3170A>G	ENSP00000506226.1:p.His1057Arg
ENST00000679714.1:c.3179A>G	ENSP00000506627.1:p.His1060Arg
ENST00000679757.1:c.2834A>G	ENSP00000505158.1:p.His945Arg
ENST00000679858.1:c.*2567A>G	ENSP00000505655.1:n.*2567A>G
ENST00000680211.1:c.-215A>G	ENSP00000506102.1:n.-215A>G
ENST00000680349.1:n.1168A>G
ENST00000680403.1:c.3185A>G	ENSP00000505677.1:p.His1062Arg
ENST00000680564.1:c.2972-621A>G	ENSP00000505582.1:n.2972-621A>G
ENST00000680590.1:c.*1580A>G	ENSP00000505350.1:n.*1580A>G
ENST00000680739.1:c.103A>G
ENST00000680773.1:n.1101A>G
ENST00000680806.1:c.*1903A>G	ENSP00000506418.1:n.*1903A>G
ENST00000680997.1:n.532A>G
ENST00000681088.1:c.847A>G
ENST00000681608.1:n.133A>G
ENST00000681625.1:c.*517A>G	ENSP00000505555.1:n.*517A>G
ENST00000270301.11:c.3185A>G	ENSP00000270301.6:p.His1062Arg
ENST00000401500.6:c.3185A>G	ENSP00000384792.1:p.His1062Arg
ENST00000587391.5:c.*2460A>G	ENSP00000465525.1:n.*2460A>G
NM_001083961.1:c.3185A>G	NP_001077430.1:p.His1062Arg
NM_173636.4:c.3185A>G	NP_775907.4:p.His1062Arg
XM_005258809.2:c.3074A>G	XP_005258866.1:p.His1025Arg
XM_011526837.1:c.3170A>G	XP_011525139.1:p.His1057Arg
XM_011526838.1:c.2972-621A>G	XP_011525140.1:n.2972-621A>G
XM_011526839.1:c.2834A>G	XP_011525141.1:p.His945Arg
XM_011526840.1:c.2177A>G	XP_011525142.1:p.His726Arg
XM_011526841.1:c.1763A>G	XP_011525143.1:p.His588Arg
XM_011526842.1:c.1616A>G	XP_011525144.1:p.His539Arg
XM_011526843.1:c.932A>G	XP_011525145.1:p.His311Arg
XM_011526844.1:c.932A>G	XP_011525146.1:p.His311Arg
XM_011526840.2:c.2177A>G	XP_011525142.1:p.His726Arg
XM_011526841.2:c.1763A>G	XP_011525143.1:p.His588Arg
XM_011526844.2:c.932A>G	XP_011525146.1:p.His311Arg
XM_017026665.1:c.3185A>G	XP_016882154.1:p.His1062Arg
NM_001083961.2:c.3185A>G MANE Select	NP_001077430.1:p.His1062Arg
NM_173636.5:c.3185A>G	NP_775907.4:p.His1062Arg