Canonical Allele Identifier: CA442557491

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210551T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289398T>G , CM000666.2:g.183289398T>G	GRCh38
NC_000004.11:g.184210551T>G , CM000666.1:g.184210551T>G	GRCh37
NC_000004.10:g.184447545T>G	NCBI36
NG_051586.1:g.195764T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3147T>G MANE Select	ENSP00000384222.3:p.Val1049=
ENST00000403733.7:c.3147T>G	ENSP00000384222.3:p.Val1049=
ENST00000427431.5:c.*2539T>G	ENSP00000393342.1:n.*2539T>G
ENST00000438543.5:c.*943T>G	ENSP00000413521.1:n.*943T>G
ENST00000448232.6:c.3219T>G	ENSP00000398577.2:p.Val1073=
ENST00000504005.5:c.2193T>G	ENSP00000427569.1:p.Val731=
ENST00000508747.1:c.531T>G	ENSP00000420835.1:p.Val177=
ENST00000513834.5:c.3000T>G	ENSP00000425054.1:p.Val1000=
NM_024949.5:c.3147T>G	NP_079225.5:p.Val1049=
XM_011532269.1:c.3219T>G	XP_011530571.1:p.Val1073=
XM_011532269.3:c.3219T>G	XP_011530571.1:p.Val1073=
XM_024454225.1:c.2925T>G	XP_024309993.1:p.Val975=
NM_024949.6:c.3147T>G MANE Select	NP_079225.5:p.Val1049=