Canonical Allele Identifier: CA405450791

Gene: WDR62

Linked Data

• dbSNP Id: rs1183521114
• gnomAD v3: 19-36102128-C-T
• gnomAD v4: 19-36102128-C-T
• MyVariant Identifiers: chr19:g.36593030C>T (hg19) ; chr19:g.36102128C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102128C>T , CM000681.2:g.36102128C>T	GRCh38
NC_000019.9:g.36593030C>T , CM000681.1:g.36593030C>T	GRCh37
NC_000019.8:g.41284870C>T	NCBI36
NG_028101.1:g.52248C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3197C>T	ENSP00000270301.6:p.Thr1066Ile
ENST00000401500.7:c.3197C>T MANE Select	ENSP00000384792.1:p.Thr1066Ile
ENST00000587391.6:c.*2472C>T	ENSP00000465525.1:n.*2472C>T
ENST00000679357.1:c.987C>T
ENST00000679422.1:c.876C>T
ENST00000679682.1:c.3182C>T	ENSP00000506226.1:p.Thr1061Ile
ENST00000679714.1:c.3191C>T	ENSP00000506627.1:p.Thr1064Ile
ENST00000679757.1:c.2846C>T	ENSP00000505158.1:p.Thr949Ile
ENST00000679858.1:c.*2579C>T	ENSP00000505655.1:n.*2579C>T
ENST00000680211.1:c.-203C>T	ENSP00000506102.1:n.-203C>T
ENST00000680349.1:n.1180C>T
ENST00000680403.1:c.3197C>T	ENSP00000505677.1:p.Thr1066Ile
ENST00000680564.1:c.2972-609C>T	ENSP00000505582.1:n.2972-609C>T
ENST00000680590.1:c.*1592C>T	ENSP00000505350.1:n.*1592C>T
ENST00000680739.1:c.115C>T
ENST00000680773.1:n.1113C>T
ENST00000680806.1:c.*1915C>T	ENSP00000506418.1:n.*1915C>T
ENST00000680997.1:n.544C>T
ENST00000681088.1:c.859C>T
ENST00000681608.1:n.145C>T
ENST00000681625.1:c.*529C>T	ENSP00000505555.1:n.*529C>T
ENST00000270301.11:c.3197C>T	ENSP00000270301.6:p.Thr1066Ile
ENST00000401500.6:c.3197C>T	ENSP00000384792.1:p.Thr1066Ile
ENST00000587391.5:c.*2472C>T	ENSP00000465525.1:n.*2472C>T
NM_001083961.1:c.3197C>T	NP_001077430.1:p.Thr1066Ile
NM_173636.4:c.3197C>T	NP_775907.4:p.Thr1066Ile
XM_005258809.2:c.3086C>T	XP_005258866.1:p.Thr1029Ile
XM_011526837.1:c.3182C>T	XP_011525139.1:p.Thr1061Ile
XM_011526838.1:c.2972-609C>T	XP_011525140.1:n.2972-609C>T
XM_011526839.1:c.2846C>T	XP_011525141.1:p.Thr949Ile
XM_011526840.1:c.2189C>T	XP_011525142.1:p.Thr730Ile
XM_011526841.1:c.1775C>T	XP_011525143.1:p.Thr592Ile
XM_011526842.1:c.1628C>T	XP_011525144.1:p.Thr543Ile
XM_011526843.1:c.944C>T	XP_011525145.1:p.Thr315Ile
XM_011526844.1:c.944C>T	XP_011525146.1:p.Thr315Ile
XM_011526840.2:c.2189C>T	XP_011525142.1:p.Thr730Ile
XM_011526841.2:c.1775C>T	XP_011525143.1:p.Thr592Ile
XM_011526844.2:c.944C>T	XP_011525146.1:p.Thr315Ile
XM_017026665.1:c.3197C>T	XP_016882154.1:p.Thr1066Ile
NM_001083961.2:c.3197C>T MANE Select	NP_001077430.1:p.Thr1066Ile
NM_173636.5:c.3197C>T	NP_775907.4:p.Thr1066Ile