Canonical Allele Identifier: CA632786902

Gene: WDR62

Linked Data

• dbSNP Id: rs1319120530
• gnomAD v2: 19-36592680-A-G
• gnomAD v3: 19-36101778-A-G
• gnomAD v4: 19-36101778-A-G
• MyVariant Identifiers: chr19:g.36592680A>G (hg19) ; chr19:g.36101778A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36101778A>G , CM000681.2:g.36101778A>G	GRCh38
NC_000019.9:g.36592680A>G , CM000681.1:g.36592680A>G	GRCh37
NC_000019.8:g.41284520A>G	NCBI36
NG_028101.1:g.51898A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3082+4A>G	ENSP00000270301.6:n.3082+4A>G
ENST00000401500.7:c.3082+4A>G MANE Select	ENSP00000384792.1:n.3082+4A>G
ENST00000587391.6:c.*2122A>G	ENSP00000465525.1:n.*2122A>G
ENST00000679357.1:c.872+4A>G
ENST00000679422.1:c.762-236A>G
ENST00000679682.1:c.3067+4A>G	ENSP00000506226.1:n.3067+4A>G
ENST00000679714.1:c.3076+4A>G	ENSP00000506627.1:n.3076+4A>G
ENST00000679757.1:c.2731+4A>G	ENSP00000505158.1:n.2731+4A>G
ENST00000679858.1:c.*2229A>G	ENSP00000505655.1:n.*2229A>G
ENST00000680211.1:c.-318+4A>G	ENSP00000506102.1:n.-318+4A>G
ENST00000680349.1:n.1065+4A>G
ENST00000680403.1:c.3082+4A>G	ENSP00000505677.1:n.3082+4A>G
ENST00000680564.1:c.2971+461A>G	ENSP00000505582.1:n.2971+461A>G
ENST00000680590.1:c.*1477+4A>G	ENSP00000505350.1:n.*1477+4A>G
ENST00000680773.1:n.763A>G
ENST00000680806.1:c.*1801-236A>G	ENSP00000506418.1:n.*1801-236A>G
ENST00000680997.1:n.429+4A>G
ENST00000681088.1:c.744+4A>G
ENST00000681608.1:n.30+4A>G
ENST00000681625.1:c.*414+4A>G	ENSP00000505555.1:n.*414+4A>G
ENST00000270301.11:c.3082+4A>G	ENSP00000270301.6:n.3082+4A>G
ENST00000401500.6:c.3082+4A>G	ENSP00000384792.1:n.3082+4A>G
ENST00000587391.5:c.*2122A>G	ENSP00000465525.1:n.*2122A>G
NM_001083961.1:c.3082+4A>G	NP_001077430.1:n.3082+4A>G
NM_173636.4:c.3082+4A>G	NP_775907.4:n.3082+4A>G
XM_005258809.2:c.2972-236A>G	XP_005258866.1:n.2972-236A>G
XM_011526837.1:c.3067+4A>G	XP_011525139.1:n.3067+4A>G
XM_011526838.1:c.2971+461A>G	XP_011525140.1:n.2971+461A>G
XM_011526839.1:c.2731+4A>G	XP_011525141.1:n.2731+4A>G
XM_011526840.1:c.2074+4A>G	XP_011525142.1:n.2074+4A>G
XM_011526841.1:c.1660+4A>G	XP_011525143.1:n.1660+4A>G
XM_011526842.1:c.1513+4A>G	XP_011525144.1:n.1513+4A>G
XM_011526843.1:c.829+4A>G	XP_011525145.1:n.829+4A>G
XM_011526844.1:c.829+4A>G	XP_011525146.1:n.829+4A>G
XM_011526840.2:c.2074+4A>G	XP_011525142.1:n.2074+4A>G
XM_011526841.2:c.1660+4A>G	XP_011525143.1:n.1660+4A>G
XM_011526844.2:c.829+4A>G	XP_011525146.1:n.829+4A>G
XM_017026665.1:c.3082+4A>G	XP_016882154.1:n.3082+4A>G
NM_001083961.2:c.3082+4A>G MANE Select	NP_001077430.1:n.3082+4A>G
NM_173636.5:c.3082+4A>G	NP_775907.4:n.3082+4A>G