Canonical Allele Identifier: CA307842364

Gene: WDR62

Linked Data

• dbSNP Id: rs760551208
• gnomAD v4: 19-36102961-T-G
• MyVariant Identifiers: chr19:g.36593863T>G (hg19) ; chr19:g.36102961T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36102961T>G , CM000681.2:g.36102961T>G	GRCh38
NC_000019.9:g.36593863T>G , CM000681.1:g.36593863T>G	GRCh37
NC_000019.8:g.41285703T>G	NCBI36
NG_028101.1:g.53081T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000270301.12:c.3334T>G	ENSP00000270301.6:p.Phe1112Val
ENST00000401500.7:c.3349T>G MANE Select	ENSP00000384792.1:p.Phe1117Val
ENST00000587391.6:c.*3209T>G	ENSP00000465525.1:n.*3209T>G
ENST00000679357.1:c.1429T>G
ENST00000679598.1:c.114T>G
ENST00000679682.1:c.3334T>G	ENSP00000506226.1:p.Phe1112Val
ENST00000679714.1:c.3343T>G	ENSP00000506627.1:p.Phe1115Val
ENST00000679757.1:c.2998T>G	ENSP00000505158.1:p.Phe1000Val
ENST00000679858.1:c.*2731T>G	ENSP00000505655.1:n.*2731T>G
ENST00000680211.1:c.-51T>G	ENSP00000506102.1:n.-51T>G
ENST00000680280.1:n.636T>G
ENST00000680349.1:n.1917T>G
ENST00000680403.1:c.3334T>G	ENSP00000505677.1:p.Phe1112Val
ENST00000680564.1:c.3100T>G	ENSP00000505582.1:p.Phe1034Val
ENST00000680590.1:c.*1729T>G	ENSP00000505350.1:n.*1729T>G
ENST00000680597.1:c.114T>G
ENST00000680739.1:c.364T>G
ENST00000680773.1:n.1850T>G
ENST00000680806.1:c.*2652T>G	ENSP00000506418.1:n.*2652T>G
ENST00000680997.1:n.1281T>G
ENST00000681608.1:n.978T>G
ENST00000681625.1:c.*681T>G	ENSP00000505555.1:n.*681T>G
ENST00000681648.1:n.648T>G
ENST00000270301.11:c.3334T>G	ENSP00000270301.6:p.Phe1112Val
ENST00000401500.6:c.3349T>G	ENSP00000384792.1:p.Phe1117Val
ENST00000587391.5:c.*3209T>G	ENSP00000465525.1:n.*3209T>G
NM_001083961.1:c.3349T>G	NP_001077430.1:p.Phe1117Val
NM_173636.4:c.3334T>G	NP_775907.4:p.Phe1112Val
XM_005258809.2:c.3238T>G	XP_005258866.1:p.Phe1080Val
XM_011526837.1:c.3334T>G	XP_011525139.1:p.Phe1112Val
XM_011526838.1:c.3100T>G	XP_011525140.1:p.Phe1034Val
XM_011526839.1:c.2998T>G	XP_011525141.1:p.Phe1000Val
XM_011526840.1:c.2341T>G	XP_011525142.1:p.Phe781Val
XM_011526841.1:c.1927T>G	XP_011525143.1:p.Phe643Val
XM_011526842.1:c.1780T>G	XP_011525144.1:p.Phe594Val
XM_011526843.1:c.1096T>G	XP_011525145.1:p.Phe366Val
XM_011526844.1:c.1096T>G	XP_011525146.1:p.Phe366Val
XM_011526840.2:c.2341T>G	XP_011525142.1:p.Phe781Val
XM_011526841.2:c.1927T>G	XP_011525143.1:p.Phe643Val
XM_011526844.2:c.1096T>G	XP_011525146.1:p.Phe366Val
XM_017026665.1:c.3349T>G	XP_016882154.1:p.Phe1117Val
NM_001083961.2:c.3349T>G MANE Select	NP_001077430.1:p.Phe1117Val
NM_173636.5:c.3334T>G	NP_775907.4:p.Phe1112Val