Canonical Allele Identifier: CA9396180

Gene: WDR62

Linked Data

• dbSNP Id: rs377379107
• ExAC: 19:36593031 A / G
• gnomAD v2: 19-36593031-A-G
• gnomAD v3: 19-36102129-A-G
• gnomAD v4: 19-36102129-A-G
• MyVariant Identifiers: chr19:g.36593031A>G (hg19) ; chr19:g.36102129A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102129A>G , CM000681.2:g.36102129A>G	GRCh38
NC_000019.9:g.36593031A>G , CM000681.1:g.36593031A>G	GRCh37
NC_000019.8:g.41284871A>G	NCBI36
NG_028101.1:g.52249A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3198A>G	ENSP00000270301.6:p.Thr1066=
ENST00000401500.7:c.3198A>G MANE Select	ENSP00000384792.1:p.Thr1066=
ENST00000587391.6:c.*2473A>G	ENSP00000465525.1:n.*2473A>G
ENST00000679357.1:c.988A>G
ENST00000679422.1:c.877A>G
ENST00000679682.1:c.3183A>G	ENSP00000506226.1:p.Thr1061=
ENST00000679714.1:c.3192A>G	ENSP00000506627.1:p.Thr1064=
ENST00000679757.1:c.2847A>G	ENSP00000505158.1:p.Thr949=
ENST00000679858.1:c.*2580A>G	ENSP00000505655.1:n.*2580A>G
ENST00000680211.1:c.-202A>G	ENSP00000506102.1:n.-202A>G
ENST00000680349.1:n.1181A>G
ENST00000680403.1:c.3198A>G	ENSP00000505677.1:p.Thr1066=
ENST00000680564.1:c.2972-608A>G	ENSP00000505582.1:n.2972-608A>G
ENST00000680590.1:c.*1593A>G	ENSP00000505350.1:n.*1593A>G
ENST00000680739.1:c.116A>G
ENST00000680773.1:n.1114A>G
ENST00000680806.1:c.*1916A>G	ENSP00000506418.1:n.*1916A>G
ENST00000680997.1:n.545A>G
ENST00000681088.1:c.860A>G
ENST00000681608.1:n.146A>G
ENST00000681625.1:c.*530A>G	ENSP00000505555.1:n.*530A>G
ENST00000270301.11:c.3198A>G	ENSP00000270301.6:p.Thr1066=
ENST00000401500.6:c.3198A>G	ENSP00000384792.1:p.Thr1066=
ENST00000587391.5:c.*2473A>G	ENSP00000465525.1:n.*2473A>G
NM_001083961.1:c.3198A>G	NP_001077430.1:p.Thr1066=
NM_173636.4:c.3198A>G	NP_775907.4:p.Thr1066=
XM_005258809.2:c.3087A>G	XP_005258866.1:p.Thr1029=
XM_011526837.1:c.3183A>G	XP_011525139.1:p.Thr1061=
XM_011526838.1:c.2972-608A>G	XP_011525140.1:n.2972-608A>G
XM_011526839.1:c.2847A>G	XP_011525141.1:p.Thr949=
XM_011526840.1:c.2190A>G	XP_011525142.1:p.Thr730=
XM_011526841.1:c.1776A>G	XP_011525143.1:p.Thr592=
XM_011526842.1:c.1629A>G	XP_011525144.1:p.Thr543=
XM_011526843.1:c.945A>G	XP_011525145.1:p.Thr315=
XM_011526844.1:c.945A>G	XP_011525146.1:p.Thr315=
XM_011526840.2:c.2190A>G	XP_011525142.1:p.Thr730=
XM_011526841.2:c.1776A>G	XP_011525143.1:p.Thr592=
XM_011526844.2:c.945A>G	XP_011525146.1:p.Thr315=
XM_017026665.1:c.3198A>G	XP_016882154.1:p.Thr1066=
NM_001083961.2:c.3198A>G MANE Select	NP_001077430.1:p.Thr1066=
NM_173636.5:c.3198A>G	NP_775907.4:p.Thr1066=