Canonical Allele Identifier: CA358845991

Gene: WWC2

Linked Data

• dbSNP Id: rs1341045338
• gnomAD v2: 4-184210642-C-A
• gnomAD v4: 4-183289489-C-A
• MyVariant Identifiers: chr4:g.184210642C>A (hg19) ; chr4:g.183289489C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289489C>A , CM000666.2:g.183289489C>A	GRCh38
NC_000004.11:g.184210642C>A , CM000666.1:g.184210642C>A	GRCh37
NC_000004.10:g.184447636C>A	NCBI36
NG_051586.1:g.195855C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3238C>A MANE Select	ENSP00000384222.3:p.Gln1080Lys
ENST00000403733.7:c.3238C>A	ENSP00000384222.3:p.Gln1080Lys
ENST00000427431.5:c.*2630C>A	ENSP00000393342.1:n.*2630C>A
ENST00000438543.5:c.*1034C>A	ENSP00000413521.1:n.*1034C>A
ENST00000448232.6:c.3310C>A	ENSP00000398577.2:p.Gln1104Lys
ENST00000504005.5:c.2284C>A	ENSP00000427569.1:p.Gln762Lys
ENST00000508747.1:c.622C>A	ENSP00000420835.1:p.Gln208Lys
ENST00000513834.5:c.3091C>A	ENSP00000425054.1:p.Gln1031Lys
NM_024949.5:c.3238C>A	NP_079225.5:p.Gln1080Lys
XM_011532269.1:c.3310C>A	XP_011530571.1:p.Gln1104Lys
XM_011532269.3:c.3310C>A	XP_011530571.1:p.Gln1104Lys
XM_024454225.1:c.3016C>A	XP_024309993.1:p.Gln1006Lys
NM_024949.6:c.3238C>A MANE Select	NP_079225.5:p.Gln1080Lys