Canonical Allele Identifier: CA3150306
Gene: WWC2 HGNC NCBI

Linked Data

dbSNP Id: rs764266153

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