Canonical Allele Identifier: CA9396188

Gene: WDR62

Linked Data

• ClinVar Variation Id: 1636119
• ClinVar RCV Id: RCV002135386
• dbSNP Id: rs374931139
• ExAC: 19:36593061 C / T
• gnomAD v2: 19-36593061-C-T
• gnomAD v3: 19-36102159-C-T
• gnomAD v4: 19-36102159-C-T
• MyVariant Identifiers: chr19:g.36593061C>T (hg19) ; chr19:g.36102159C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102159C>T , CM000681.2:g.36102159C>T	GRCh38
NC_000019.9:g.36593061C>T , CM000681.1:g.36593061C>T	GRCh37
NC_000019.8:g.41284901C>T	NCBI36
NG_028101.1:g.52279C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3220+8C>T	ENSP00000270301.6:n.3220+8C>T
ENST00000401500.7:c.3220+8C>T MANE Select	ENSP00000384792.1:n.3220+8C>T
ENST00000587391.6:c.*2503C>T	ENSP00000465525.1:n.*2503C>T
ENST00000679357.1:c.1010+8C>T
ENST00000679682.1:c.3205+8C>T	ENSP00000506226.1:n.3205+8C>T
ENST00000679714.1:c.3214+8C>T	ENSP00000506627.1:n.3214+8C>T
ENST00000679757.1:c.2869+8C>T	ENSP00000505158.1:n.2869+8C>T
ENST00000679858.1:c.*2602+8C>T	ENSP00000505655.1:n.*2602+8C>T
ENST00000680211.1:c.-180+8C>T	ENSP00000506102.1:n.-180+8C>T
ENST00000680349.1:n.1211C>T
ENST00000680403.1:c.3220+8C>T	ENSP00000505677.1:n.3220+8C>T
ENST00000680564.1:c.2972-578C>T	ENSP00000505582.1:n.2972-578C>T
ENST00000680590.1:c.*1615+8C>T	ENSP00000505350.1:n.*1615+8C>T
ENST00000680739.1:c.146C>T
ENST00000680773.1:n.1144C>T
ENST00000680806.1:c.*1946C>T	ENSP00000506418.1:n.*1946C>T
ENST00000680997.1:n.575C>T
ENST00000681608.1:n.176C>T
ENST00000681625.1:c.*552+8C>T	ENSP00000505555.1:n.*552+8C>T
ENST00000270301.11:c.3220+8C>T	ENSP00000270301.6:n.3220+8C>T
ENST00000401500.6:c.3220+8C>T	ENSP00000384792.1:n.3220+8C>T
ENST00000587391.5:c.*2503C>T	ENSP00000465525.1:n.*2503C>T
NM_001083961.1:c.3220+8C>T	NP_001077430.1:n.3220+8C>T
NM_173636.4:c.3220+8C>T	NP_775907.4:n.3220+8C>T
XM_005258809.2:c.3109+8C>T	XP_005258866.1:n.3109+8C>T
XM_011526837.1:c.3205+8C>T	XP_011525139.1:n.3205+8C>T
XM_011526838.1:c.2972-578C>T	XP_011525140.1:n.2972-578C>T
XM_011526839.1:c.2869+8C>T	XP_011525141.1:n.2869+8C>T
XM_011526840.1:c.2212+8C>T	XP_011525142.1:n.2212+8C>T
XM_011526841.1:c.1798+8C>T	XP_011525143.1:n.1798+8C>T
XM_011526842.1:c.1651+8C>T	XP_011525144.1:n.1651+8C>T
XM_011526843.1:c.967+8C>T	XP_011525145.1:n.967+8C>T
XM_011526844.1:c.967+8C>T	XP_011525146.1:n.967+8C>T
XM_011526840.2:c.2212+8C>T	XP_011525142.1:n.2212+8C>T
XM_011526841.2:c.1798+8C>T	XP_011525143.1:n.1798+8C>T
XM_011526844.2:c.967+8C>T	XP_011525146.1:n.967+8C>T
XM_017026665.1:c.3220+8C>T	XP_016882154.1:n.3220+8C>T
NM_001083961.2:c.3220+8C>T MANE Select	NP_001077430.1:n.3220+8C>T
NM_173636.5:c.3220+8C>T	NP_775907.4:n.3220+8C>T