Canonical Allele Identifier: CA405461136

Gene: WDR62

Linked Data

• dbSNP Id: rs1973626751
• gnomAD v4: 19-36104629-A-G
• MyVariant Identifiers: chr19:g.36595531A>G (hg19) ; chr19:g.36104629A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104629A>G , CM000681.2:g.36104629A>G	GRCh38
NC_000019.9:g.36595531A>G , CM000681.1:g.36595531A>G	GRCh37
NC_000019.8:g.41287371A>G	NCBI36
NG_028101.1:g.54749A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4250A>G	ENSP00000270301.6:p.His1417Arg
ENST00000401500.7:c.4265A>G MANE Select	ENSP00000384792.1:p.His1422Arg
ENST00000587391.6:c.*4125A>G	ENSP00000465525.1:n.*4125A>G
ENST00000679357.1:c.2345A>G
ENST00000679598.1:c.1010A>G
ENST00000679682.1:c.4250A>G	ENSP00000506226.1:p.His1417Arg
ENST00000679714.1:c.4259A>G	ENSP00000506627.1:p.His1420Arg
ENST00000679757.1:c.3914A>G	ENSP00000505158.1:p.His1305Arg
ENST00000679858.1:c.*3647A>G	ENSP00000505655.1:n.*3647A>G
ENST00000680211.1:c.866A>G	ENSP00000506102.1:p.His289Arg
ENST00000680280.1:n.1768A>G
ENST00000680349.1:n.2914A>G
ENST00000680403.1:c.4250A>G	ENSP00000505677.1:p.His1417Arg
ENST00000680564.1:c.4016A>G	ENSP00000505582.1:p.His1339Arg
ENST00000680590.1:c.*2645A>G	ENSP00000505350.1:n.*2645A>G
ENST00000680597.1:c.998A>G
ENST00000680739.1:c.1280A>G
ENST00000680773.1:n.2766A>G
ENST00000680806.1:c.*3568A>G	ENSP00000506418.1:n.*3568A>G
ENST00000680997.1:n.2197A>G
ENST00000681608.1:n.2110A>G
ENST00000681625.1:c.*1597A>G	ENSP00000505555.1:n.*1597A>G
ENST00000681648.1:n.2316A>G
ENST00000270301.11:c.4250A>G	ENSP00000270301.6:p.His1417Arg
ENST00000401500.6:c.4265A>G	ENSP00000384792.1:p.His1422Arg
ENST00000587391.5:c.*4125A>G	ENSP00000465525.1:n.*4125A>G
NM_001083961.1:c.4265A>G	NP_001077430.1:p.His1422Arg
NM_173636.4:c.4250A>G	NP_775907.4:p.His1417Arg
XM_005258809.2:c.4154A>G	XP_005258866.1:p.His1385Arg
XM_011526837.1:c.4250A>G	XP_011525139.1:p.His1417Arg
XM_011526838.1:c.4016A>G	XP_011525140.1:p.His1339Arg
XM_011526839.1:c.3914A>G	XP_011525141.1:p.His1305Arg
XM_011526840.1:c.3257A>G	XP_011525142.1:p.His1086Arg
XM_011526841.1:c.2843A>G	XP_011525143.1:p.His948Arg
XM_011526842.1:c.2696A>G	XP_011525144.1:p.His899Arg
XM_011526843.1:c.2012A>G	XP_011525145.1:p.His671Arg
XM_011526844.1:c.2012A>G	XP_011525146.1:p.His671Arg
XM_011526840.2:c.3257A>G	XP_011525142.1:p.His1086Arg
XM_011526841.2:c.2843A>G	XP_011525143.1:p.His948Arg
XM_011526844.2:c.2012A>G	XP_011525146.1:p.His671Arg
XM_017026665.1:c.4265A>G	XP_016882154.1:p.His1422Arg
NM_001083961.2:c.4265A>G MANE Select	NP_001077430.1:p.His1422Arg
NM_173636.5:c.4250A>G	NP_775907.4:p.His1417Arg