Canonical Allele Identifier: CA3150306

Gene: WWC2

Linked Data

• dbSNP Id: rs764266153
• ExAC: 4:184210647 C / A
• gnomAD v2: 4-184210647-C-A
• MyVariant Identifiers: chr4:g.184210647C>A (hg19) ; chr4:g.183289494C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289494C>A , CM000666.2:g.183289494C>A	GRCh38
NC_000004.11:g.184210647C>A , CM000666.1:g.184210647C>A	GRCh37
NC_000004.10:g.184447641C>A	NCBI36
NG_051586.1:g.195860C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3243C>A MANE Select	ENSP00000384222.3:p.Ser1081Arg
ENST00000403733.7:c.3243C>A	ENSP00000384222.3:p.Ser1081Arg
ENST00000427431.5:c.*2635C>A	ENSP00000393342.1:n.*2635C>A
ENST00000438543.5:c.*1039C>A	ENSP00000413521.1:n.*1039C>A
ENST00000448232.6:c.3315C>A	ENSP00000398577.2:p.Ser1105Arg
ENST00000504005.5:c.2289C>A	ENSP00000427569.1:p.Ser763Arg
ENST00000508747.1:c.627C>A	ENSP00000420835.1:p.Ser209Arg
ENST00000513834.5:c.3096C>A	ENSP00000425054.1:p.Ser1032Arg
NM_024949.5:c.3243C>A	NP_079225.5:p.Ser1081Arg
XM_011532269.1:c.3315C>A	XP_011530571.1:p.Ser1105Arg
XM_011532269.3:c.3315C>A	XP_011530571.1:p.Ser1105Arg
XM_024454225.1:c.3021C>A	XP_024309993.1:p.Ser1007Arg
NM_024949.6:c.3243C>A MANE Select	NP_079225.5:p.Ser1081Arg