Canonical Allele Identifier: CA881853807

Gene: WDR62

Linked Data

• dbSNP Id: rs1255902268
• gnomAD v3: 19-36104240-A-G
• gnomAD v4: 19-36104240-A-G
• MyVariant Identifiers: chr19:g.36595142A>G (hg19) ; chr19:g.36104240A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104240A>G , CM000681.2:g.36104240A>G	GRCh38
NC_000019.9:g.36595142A>G , CM000681.1:g.36595142A>G	GRCh37
NC_000019.8:g.41286982A>G	NCBI36
NG_028101.1:g.54360A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4138+259A>G	ENSP00000270301.6:n.4138+259A>G
ENST00000401500.7:c.4153+259A>G MANE Select	ENSP00000384792.1:n.4153+259A>G
ENST00000587391.6:c.*4013+259A>G	ENSP00000465525.1:n.*4013+259A>G
ENST00000679357.1:c.2233+259A>G
ENST00000679598.1:c.918+259A>G
ENST00000679682.1:c.4138+259A>G	ENSP00000506226.1:n.4138+259A>G
ENST00000679714.1:c.4147+259A>G	ENSP00000506627.1:n.4147+259A>G
ENST00000679757.1:c.3802+259A>G	ENSP00000505158.1:n.3802+259A>G
ENST00000679858.1:c.*3535+259A>G	ENSP00000505655.1:n.*3535+259A>G
ENST00000680211.1:c.754+259A>G	ENSP00000506102.1:n.754+259A>G
ENST00000680280.1:n.1656+259A>G
ENST00000680349.1:n.2802+259A>G
ENST00000680403.1:c.4138+259A>G	ENSP00000505677.1:n.4138+259A>G
ENST00000680564.1:c.3904+259A>G	ENSP00000505582.1:n.3904+259A>G
ENST00000680590.1:c.*2533+259A>G	ENSP00000505350.1:n.*2533+259A>G
ENST00000680597.1:c.886+259A>G
ENST00000680739.1:c.1168+259A>G
ENST00000680773.1:n.2654+259A>G
ENST00000680806.1:c.*3456+259A>G	ENSP00000506418.1:n.*3456+259A>G
ENST00000680997.1:n.2085+259A>G
ENST00000681608.1:n.1998+259A>G
ENST00000681625.1:c.*1485+259A>G	ENSP00000505555.1:n.*1485+259A>G
ENST00000681648.1:n.1927A>G
ENST00000270301.11:c.4138+259A>G	ENSP00000270301.6:n.4138+259A>G
ENST00000401500.6:c.4153+259A>G	ENSP00000384792.1:n.4153+259A>G
ENST00000587391.5:c.*4013+259A>G	ENSP00000465525.1:n.*4013+259A>G
NM_001083961.1:c.4153+259A>G	NP_001077430.1:n.4153+259A>G
NM_173636.4:c.4138+259A>G	NP_775907.4:n.4138+259A>G
XM_005258809.2:c.4042+259A>G	XP_005258866.1:n.4042+259A>G
XM_011526837.1:c.4138+259A>G	XP_011525139.1:n.4138+259A>G
XM_011526838.1:c.3904+259A>G	XP_011525140.1:n.3904+259A>G
XM_011526839.1:c.3802+259A>G	XP_011525141.1:n.3802+259A>G
XM_011526840.1:c.3145+259A>G	XP_011525142.1:n.3145+259A>G
XM_011526841.1:c.2731+259A>G	XP_011525143.1:n.2731+259A>G
XM_011526842.1:c.2584+259A>G	XP_011525144.1:n.2584+259A>G
XM_011526843.1:c.1900+259A>G	XP_011525145.1:n.1900+259A>G
XM_011526844.1:c.1900+259A>G	XP_011525146.1:n.1900+259A>G
XM_011526840.2:c.3145+259A>G	XP_011525142.1:n.3145+259A>G
XM_011526841.2:c.2731+259A>G	XP_011525143.1:n.2731+259A>G
XM_011526844.2:c.1900+259A>G	XP_011525146.1:n.1900+259A>G
XM_017026665.1:c.4153+259A>G	XP_016882154.1:n.4153+259A>G
NM_001083961.2:c.4153+259A>G MANE Select	NP_001077430.1:n.4153+259A>G
NM_173636.5:c.4138+259A>G	NP_775907.4:n.4138+259A>G