Canonical Allele Identifier: CA881853813

Gene: WDR62

Linked Data

• dbSNP Id: rs1307248385
• gnomAD v3: 19-36104250-C-T
• gnomAD v4: 19-36104250-C-T
• MyVariant Identifiers: chr19:g.36595152C>T (hg19) ; chr19:g.36104250C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.36104250C>T , CM000681.2:g.36104250C>T	GRCh38
NC_000019.9:g.36595152C>T , CM000681.1:g.36595152C>T	GRCh37
NC_000019.8:g.41286992C>T	NCBI36
NG_028101.1:g.54370C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000270301.12:c.4139-268C>T	ENSP00000270301.6:n.4139-268C>T
ENST00000401500.7:c.4154-268C>T MANE Select	ENSP00000384792.1:n.4154-268C>T
ENST00000587391.6:c.*4014-268C>T	ENSP00000465525.1:n.*4014-268C>T
ENST00000679357.1:c.2234-268C>T
ENST00000679598.1:c.918+269C>T
ENST00000679682.1:c.4139-268C>T	ENSP00000506226.1:n.4139-268C>T
ENST00000679714.1:c.4148-268C>T	ENSP00000506627.1:n.4148-268C>T
ENST00000679757.1:c.3803-268C>T	ENSP00000505158.1:n.3803-268C>T
ENST00000679858.1:c.*3536-268C>T	ENSP00000505655.1:n.*3536-268C>T
ENST00000680211.1:c.755-268C>T	ENSP00000506102.1:n.755-268C>T
ENST00000680280.1:n.1657-268C>T
ENST00000680349.1:n.2803-268C>T
ENST00000680403.1:c.4139-268C>T	ENSP00000505677.1:n.4139-268C>T
ENST00000680564.1:c.3905-268C>T	ENSP00000505582.1:n.3905-268C>T
ENST00000680590.1:c.*2534-268C>T	ENSP00000505350.1:n.*2534-268C>T
ENST00000680597.1:c.887-268C>T
ENST00000680739.1:c.1169-268C>T
ENST00000680773.1:n.2655-268C>T
ENST00000680806.1:c.*3457-268C>T	ENSP00000506418.1:n.*3457-268C>T
ENST00000680997.1:n.2086-268C>T
ENST00000681608.1:n.1999-268C>T
ENST00000681625.1:c.*1486-268C>T	ENSP00000505555.1:n.*1486-268C>T
ENST00000681648.1:n.1937C>T
ENST00000270301.11:c.4139-268C>T	ENSP00000270301.6:n.4139-268C>T
ENST00000401500.6:c.4154-268C>T	ENSP00000384792.1:n.4154-268C>T
ENST00000587391.5:c.*4014-268C>T	ENSP00000465525.1:n.*4014-268C>T
NM_001083961.1:c.4154-268C>T	NP_001077430.1:n.4154-268C>T
NM_173636.4:c.4139-268C>T	NP_775907.4:n.4139-268C>T
XM_005258809.2:c.4043-268C>T	XP_005258866.1:n.4043-268C>T
XM_011526837.1:c.4139-268C>T	XP_011525139.1:n.4139-268C>T
XM_011526838.1:c.3905-268C>T	XP_011525140.1:n.3905-268C>T
XM_011526839.1:c.3803-268C>T	XP_011525141.1:n.3803-268C>T
XM_011526840.1:c.3146-268C>T	XP_011525142.1:n.3146-268C>T
XM_011526841.1:c.2732-268C>T	XP_011525143.1:n.2732-268C>T
XM_011526842.1:c.2585-268C>T	XP_011525144.1:n.2585-268C>T
XM_011526843.1:c.1901-268C>T	XP_011525145.1:n.1901-268C>T
XM_011526844.1:c.1901-268C>T	XP_011525146.1:n.1901-268C>T
XM_011526840.2:c.3146-268C>T	XP_011525142.1:n.3146-268C>T
XM_011526841.2:c.2732-268C>T	XP_011525143.1:n.2732-268C>T
XM_011526844.2:c.1901-268C>T	XP_011525146.1:n.1901-268C>T
XM_017026665.1:c.4154-268C>T	XP_016882154.1:n.4154-268C>T
NM_001083961.2:c.4154-268C>T MANE Select	NP_001077430.1:n.4154-268C>T
NM_173636.5:c.4139-268C>T	NP_775907.4:n.4139-268C>T