Canonical Allele Identifier: CA507107641

Gene: WDR62

Linked Data

• dbSNP Id: rs1420349470
• gnomAD v2: 19-36593700-C-T
• gnomAD v4: 19-36102798-C-T
• MyVariant Identifiers: chr19:g.36593700C>T (hg19) ; chr19:g.36102798C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102798C>T , CM000681.2:g.36102798C>T	GRCh38
NC_000019.9:g.36593700C>T , CM000681.1:g.36593700C>T	GRCh37
NC_000019.8:g.41285540C>T	NCBI36
NG_028101.1:g.52918C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.3267C>T	ENSP00000270301.6:p.Asn1089=
ENST00000401500.7:c.3282C>T MANE Select	ENSP00000384792.1:p.Asn1094=
ENST00000587391.6:c.*3142C>T	ENSP00000465525.1:n.*3142C>T
ENST00000679357.1:c.1362C>T
ENST00000679598.1:c.47C>T
ENST00000679682.1:c.3267C>T	ENSP00000506226.1:p.Asn1089=
ENST00000679714.1:c.3276C>T	ENSP00000506627.1:p.Asn1092=
ENST00000679757.1:c.2931C>T	ENSP00000505158.1:p.Asn977=
ENST00000679858.1:c.*2664C>T	ENSP00000505655.1:n.*2664C>T
ENST00000680211.1:c.-118C>T	ENSP00000506102.1:n.-118C>T
ENST00000680280.1:n.569C>T
ENST00000680349.1:n.1850C>T
ENST00000680403.1:c.3267C>T	ENSP00000505677.1:p.Asn1089=
ENST00000680564.1:c.3033C>T	ENSP00000505582.1:p.Asn1011=
ENST00000680590.1:c.*1662C>T	ENSP00000505350.1:n.*1662C>T
ENST00000680597.1:c.47C>T
ENST00000680739.1:c.297C>T
ENST00000680773.1:n.1783C>T
ENST00000680806.1:c.*2585C>T	ENSP00000506418.1:n.*2585C>T
ENST00000680997.1:n.1214C>T
ENST00000681608.1:n.815C>T
ENST00000681625.1:c.*614C>T	ENSP00000505555.1:n.*614C>T
ENST00000681648.1:n.581C>T
ENST00000270301.11:c.3267C>T	ENSP00000270301.6:p.Asn1089=
ENST00000401500.6:c.3282C>T	ENSP00000384792.1:p.Asn1094=
ENST00000587391.5:c.*3142C>T	ENSP00000465525.1:n.*3142C>T
NM_001083961.1:c.3282C>T	NP_001077430.1:p.Asn1094=
NM_173636.4:c.3267C>T	NP_775907.4:p.Asn1089=
XM_005258809.2:c.3171C>T	XP_005258866.1:p.Asn1057=
XM_011526837.1:c.3267C>T	XP_011525139.1:p.Asn1089=
XM_011526838.1:c.3033C>T	XP_011525140.1:p.Asn1011=
XM_011526839.1:c.2931C>T	XP_011525141.1:p.Asn977=
XM_011526840.1:c.2274C>T	XP_011525142.1:p.Asn758=
XM_011526841.1:c.1860C>T	XP_011525143.1:p.Asn620=
XM_011526842.1:c.1713C>T	XP_011525144.1:p.Asn571=
XM_011526843.1:c.1029C>T	XP_011525145.1:p.Asn343=
XM_011526844.1:c.1029C>T	XP_011525146.1:p.Asn343=
XM_011526840.2:c.2274C>T	XP_011525142.1:p.Asn758=
XM_011526841.2:c.1860C>T	XP_011525143.1:p.Asn620=
XM_011526844.2:c.1029C>T	XP_011525146.1:p.Asn343=
XM_017026665.1:c.3282C>T	XP_016882154.1:p.Asn1094=
NM_001083961.2:c.3282C>T MANE Select	NP_001077430.1:p.Asn1094=
NM_173636.5:c.3267C>T	NP_775907.4:p.Asn1089=