Canonical Allele Identifier: CA442557633

Gene: WWC2

Linked Data

• gnomAD v4: 4-183289486-C-A
• MyVariant Identifiers: chr4:g.184210639C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289486C>A , CM000666.2:g.183289486C>A	GRCh38
NC_000004.11:g.184210639C>A , CM000666.1:g.184210639C>A	GRCh37
NC_000004.10:g.184447633C>A	NCBI36
NG_051586.1:g.195852C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3235C>A MANE Select	ENSP00000384222.3:p.Arg1079=
ENST00000403733.7:c.3235C>A	ENSP00000384222.3:p.Arg1079=
ENST00000427431.5:c.*2627C>A	ENSP00000393342.1:n.*2627C>A
ENST00000438543.5:c.*1031C>A	ENSP00000413521.1:n.*1031C>A
ENST00000448232.6:c.3307C>A	ENSP00000398577.2:p.Arg1103=
ENST00000504005.5:c.2281C>A	ENSP00000427569.1:p.Arg761=
ENST00000508747.1:c.619C>A	ENSP00000420835.1:p.Arg207=
ENST00000513834.5:c.3088C>A	ENSP00000425054.1:p.Arg1030=
NM_024949.5:c.3235C>A	NP_079225.5:p.Arg1079=
XM_011532269.1:c.3307C>A	XP_011530571.1:p.Arg1103=
XM_011532269.3:c.3307C>A	XP_011530571.1:p.Arg1103=
XM_024454225.1:c.3013C>A	XP_024309993.1:p.Arg1005=
NM_024949.6:c.3235C>A MANE Select	NP_079225.5:p.Arg1079=