Canonical Allele Identifier: CA633062340

Gene: WDR62

Linked Data

• dbSNP Id: rs1419459432
• gnomAD v2: 19-36595409-C-G
• gnomAD v4: 19-36104507-C-G
• MyVariant Identifiers: chr19:g.36595409C>G (hg19) ; chr19:g.36104507C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104507C>G , CM000681.2:g.36104507C>G	GRCh38
NC_000019.9:g.36595409C>G , CM000681.1:g.36595409C>G	GRCh37
NC_000019.8:g.41287249C>G	NCBI36
NG_028101.1:g.54627C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4139-11C>G	ENSP00000270301.6:n.4139-11C>G
ENST00000401500.7:c.4154-11C>G MANE Select	ENSP00000384792.1:n.4154-11C>G
ENST00000587391.6:c.*4014-11C>G	ENSP00000465525.1:n.*4014-11C>G
ENST00000679357.1:c.2234-11C>G
ENST00000679598.1:c.919-31C>G
ENST00000679682.1:c.4139-11C>G	ENSP00000506226.1:n.4139-11C>G
ENST00000679714.1:c.4148-11C>G	ENSP00000506627.1:n.4148-11C>G
ENST00000679757.1:c.3803-11C>G	ENSP00000505158.1:n.3803-11C>G
ENST00000679858.1:c.*3536-11C>G	ENSP00000505655.1:n.*3536-11C>G
ENST00000680211.1:c.755-11C>G	ENSP00000506102.1:n.755-11C>G
ENST00000680280.1:n.1657-11C>G
ENST00000680349.1:n.2803-11C>G
ENST00000680403.1:c.4139-11C>G	ENSP00000505677.1:n.4139-11C>G
ENST00000680564.1:c.3905-11C>G	ENSP00000505582.1:n.3905-11C>G
ENST00000680590.1:c.*2534-11C>G	ENSP00000505350.1:n.*2534-11C>G
ENST00000680597.1:c.887-11C>G
ENST00000680739.1:c.1169-11C>G
ENST00000680773.1:n.2655-11C>G
ENST00000680806.1:c.*3457-11C>G	ENSP00000506418.1:n.*3457-11C>G
ENST00000680997.1:n.2086-11C>G
ENST00000681608.1:n.1999-11C>G
ENST00000681625.1:c.*1486-11C>G	ENSP00000505555.1:n.*1486-11C>G
ENST00000681648.1:n.2194C>G
ENST00000270301.11:c.4139-11C>G	ENSP00000270301.6:n.4139-11C>G
ENST00000401500.6:c.4154-11C>G	ENSP00000384792.1:n.4154-11C>G
ENST00000587391.5:c.*4014-11C>G	ENSP00000465525.1:n.*4014-11C>G
NM_001083961.1:c.4154-11C>G	NP_001077430.1:n.4154-11C>G
NM_173636.4:c.4139-11C>G	NP_775907.4:n.4139-11C>G
XM_005258809.2:c.4043-11C>G	XP_005258866.1:n.4043-11C>G
XM_011526837.1:c.4139-11C>G	XP_011525139.1:n.4139-11C>G
XM_011526838.1:c.3905-11C>G	XP_011525140.1:n.3905-11C>G
XM_011526839.1:c.3803-11C>G	XP_011525141.1:n.3803-11C>G
XM_011526840.1:c.3146-11C>G	XP_011525142.1:n.3146-11C>G
XM_011526841.1:c.2732-11C>G	XP_011525143.1:n.2732-11C>G
XM_011526842.1:c.2585-11C>G	XP_011525144.1:n.2585-11C>G
XM_011526843.1:c.1901-11C>G	XP_011525145.1:n.1901-11C>G
XM_011526844.1:c.1901-11C>G	XP_011525146.1:n.1901-11C>G
XM_011526840.2:c.3146-11C>G	XP_011525142.1:n.3146-11C>G
XM_011526841.2:c.2732-11C>G	XP_011525143.1:n.2732-11C>G
XM_011526844.2:c.1901-11C>G	XP_011525146.1:n.1901-11C>G
XM_017026665.1:c.4154-11C>G	XP_016882154.1:n.4154-11C>G
NM_001083961.2:c.4154-11C>G MANE Select	NP_001077430.1:n.4154-11C>G
NM_173636.5:c.4139-11C>G	NP_775907.4:n.4139-11C>G