Canonical Allele Identifier: CA9396177

Gene: WDR62

Linked Data

• dbSNP Id: rs150778662
• ExAC: 19:36593015 G / A
• gnomAD v2: 19-36593015-G-A
• gnomAD v3: 19-36102113-G-A
• gnomAD v4: 19-36102113-G-A
• MyVariant Identifiers: chr19:g.36593015G>A (hg19) ; chr19:g.36102113G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102113G>A , CM000681.2:g.36102113G>A	GRCh38
NC_000019.9:g.36593015G>A , CM000681.1:g.36593015G>A	GRCh37
NC_000019.8:g.41284855G>A	NCBI36
NG_028101.1:g.52233G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3182G>A	ENSP00000270301.6:p.Arg1061His
ENST00000401500.7:c.3182G>A MANE Select	ENSP00000384792.1:p.Arg1061His
ENST00000587391.6:c.*2457G>A	ENSP00000465525.1:n.*2457G>A
ENST00000679357.1:c.972G>A
ENST00000679422.1:c.861G>A
ENST00000679682.1:c.3167G>A	ENSP00000506226.1:p.Arg1056His
ENST00000679714.1:c.3176G>A	ENSP00000506627.1:p.Arg1059His
ENST00000679757.1:c.2831G>A	ENSP00000505158.1:p.Arg944His
ENST00000679858.1:c.*2564G>A	ENSP00000505655.1:n.*2564G>A
ENST00000680211.1:c.-218G>A	ENSP00000506102.1:n.-218G>A
ENST00000680349.1:n.1165G>A
ENST00000680403.1:c.3182G>A	ENSP00000505677.1:p.Arg1061His
ENST00000680564.1:c.2972-624G>A	ENSP00000505582.1:n.2972-624G>A
ENST00000680590.1:c.*1577G>A	ENSP00000505350.1:n.*1577G>A
ENST00000680739.1:c.100G>A
ENST00000680773.1:n.1098G>A
ENST00000680806.1:c.*1900G>A	ENSP00000506418.1:n.*1900G>A
ENST00000680997.1:n.529G>A
ENST00000681088.1:c.844G>A
ENST00000681608.1:n.130G>A
ENST00000681625.1:c.*514G>A	ENSP00000505555.1:n.*514G>A
ENST00000270301.11:c.3182G>A	ENSP00000270301.6:p.Arg1061His
ENST00000401500.6:c.3182G>A	ENSP00000384792.1:p.Arg1061His
ENST00000587391.5:c.*2457G>A	ENSP00000465525.1:n.*2457G>A
NM_001083961.1:c.3182G>A	NP_001077430.1:p.Arg1061His
NM_173636.4:c.3182G>A	NP_775907.4:p.Arg1061His
XM_005258809.2:c.3071G>A	XP_005258866.1:p.Arg1024His
XM_011526837.1:c.3167G>A	XP_011525139.1:p.Arg1056His
XM_011526838.1:c.2972-624G>A	XP_011525140.1:n.2972-624G>A
XM_011526839.1:c.2831G>A	XP_011525141.1:p.Arg944His
XM_011526840.1:c.2174G>A	XP_011525142.1:p.Arg725His
XM_011526841.1:c.1760G>A	XP_011525143.1:p.Arg587His
XM_011526842.1:c.1613G>A	XP_011525144.1:p.Arg538His
XM_011526843.1:c.929G>A	XP_011525145.1:p.Arg310His
XM_011526844.1:c.929G>A	XP_011525146.1:p.Arg310His
XM_011526840.2:c.2174G>A	XP_011525142.1:p.Arg725His
XM_011526841.2:c.1760G>A	XP_011525143.1:p.Arg587His
XM_011526844.2:c.929G>A	XP_011525146.1:p.Arg310His
XM_017026665.1:c.3182G>A	XP_016882154.1:p.Arg1061His
NM_001083961.2:c.3182G>A MANE Select	NP_001077430.1:p.Arg1061His
NM_173636.5:c.3182G>A	NP_775907.4:p.Arg1061His