Canonical Allele Identifier: CA442557639

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210650C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289497C>G , CM000666.2:g.183289497C>G	GRCh38
NC_000004.11:g.184210650C>G , CM000666.1:g.184210650C>G	GRCh37
NC_000004.10:g.184447644C>G	NCBI36
NG_051586.1:g.195863C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3246C>G MANE Select	ENSP00000384222.3:p.Arg1082=
ENST00000403733.7:c.3246C>G	ENSP00000384222.3:p.Arg1082=
ENST00000427431.5:c.*2638C>G	ENSP00000393342.1:n.*2638C>G
ENST00000438543.5:c.*1042C>G	ENSP00000413521.1:n.*1042C>G
ENST00000448232.6:c.3318C>G	ENSP00000398577.2:p.Arg1106=
ENST00000504005.5:c.2292C>G	ENSP00000427569.1:p.Arg764=
ENST00000508747.1:c.630C>G	ENSP00000420835.1:p.Arg210=
ENST00000513834.5:c.3099C>G	ENSP00000425054.1:p.Arg1033=
NM_024949.5:c.3246C>G	NP_079225.5:p.Arg1082=
XM_011532269.1:c.3318C>G	XP_011530571.1:p.Arg1106=
XM_011532269.3:c.3318C>G	XP_011530571.1:p.Arg1106=
XM_024454225.1:c.3024C>G	XP_024309993.1:p.Arg1008=
NM_024949.6:c.3246C>G MANE Select	NP_079225.5:p.Arg1082=