Canonical Allele Identifier: CA9396178

Gene: WDR62

Linked Data

• dbSNP Id: rs779595179
• ExAC: 19:36593020 C / T
• gnomAD v2: 19-36593020-C-T
• gnomAD v4: 19-36102118-C-T
• MyVariant Identifiers: chr19:g.36593020C>T (hg19) ; chr19:g.36102118C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102118C>T , CM000681.2:g.36102118C>T	GRCh38
NC_000019.9:g.36593020C>T , CM000681.1:g.36593020C>T	GRCh37
NC_000019.8:g.41284860C>T	NCBI36
NG_028101.1:g.52238C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3187C>T	ENSP00000270301.6:p.His1063Tyr
ENST00000401500.7:c.3187C>T MANE Select	ENSP00000384792.1:p.His1063Tyr
ENST00000587391.6:c.*2462C>T	ENSP00000465525.1:n.*2462C>T
ENST00000679357.1:c.977C>T
ENST00000679422.1:c.866C>T
ENST00000679682.1:c.3172C>T	ENSP00000506226.1:p.His1058Tyr
ENST00000679714.1:c.3181C>T	ENSP00000506627.1:p.His1061Tyr
ENST00000679757.1:c.2836C>T	ENSP00000505158.1:p.His946Tyr
ENST00000679858.1:c.*2569C>T	ENSP00000505655.1:n.*2569C>T
ENST00000680211.1:c.-213C>T	ENSP00000506102.1:n.-213C>T
ENST00000680349.1:n.1170C>T
ENST00000680403.1:c.3187C>T	ENSP00000505677.1:p.His1063Tyr
ENST00000680564.1:c.2972-619C>T	ENSP00000505582.1:n.2972-619C>T
ENST00000680590.1:c.*1582C>T	ENSP00000505350.1:n.*1582C>T
ENST00000680739.1:c.105C>T
ENST00000680773.1:n.1103C>T
ENST00000680806.1:c.*1905C>T	ENSP00000506418.1:n.*1905C>T
ENST00000680997.1:n.534C>T
ENST00000681088.1:c.849C>T
ENST00000681608.1:n.135C>T
ENST00000681625.1:c.*519C>T	ENSP00000505555.1:n.*519C>T
ENST00000270301.11:c.3187C>T	ENSP00000270301.6:p.His1063Tyr
ENST00000401500.6:c.3187C>T	ENSP00000384792.1:p.His1063Tyr
ENST00000587391.5:c.*2462C>T	ENSP00000465525.1:n.*2462C>T
NM_001083961.1:c.3187C>T	NP_001077430.1:p.His1063Tyr
NM_173636.4:c.3187C>T	NP_775907.4:p.His1063Tyr
XM_005258809.2:c.3076C>T	XP_005258866.1:p.His1026Tyr
XM_011526837.1:c.3172C>T	XP_011525139.1:p.His1058Tyr
XM_011526838.1:c.2972-619C>T	XP_011525140.1:n.2972-619C>T
XM_011526839.1:c.2836C>T	XP_011525141.1:p.His946Tyr
XM_011526840.1:c.2179C>T	XP_011525142.1:p.His727Tyr
XM_011526841.1:c.1765C>T	XP_011525143.1:p.His589Tyr
XM_011526842.1:c.1618C>T	XP_011525144.1:p.His540Tyr
XM_011526843.1:c.934C>T	XP_011525145.1:p.His312Tyr
XM_011526844.1:c.934C>T	XP_011525146.1:p.His312Tyr
XM_011526840.2:c.2179C>T	XP_011525142.1:p.His727Tyr
XM_011526841.2:c.1765C>T	XP_011525143.1:p.His589Tyr
XM_011526844.2:c.934C>T	XP_011525146.1:p.His312Tyr
XM_017026665.1:c.3187C>T	XP_016882154.1:p.His1063Tyr
NM_001083961.2:c.3187C>T MANE Select	NP_001077430.1:p.His1063Tyr
NM_173636.5:c.3187C>T	NP_775907.4:p.His1063Tyr