Canonical Allele Identifier: CA442557692

Gene: WWC2

Linked Data

• dbSNP Id: rs1282290389
• gnomAD v2: 4-184210731-A-G
• gnomAD v4: 4-183289578-A-G
• MyVariant Identifiers: chr4:g.184210731A>G (hg19) ; chr4:g.183289578A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289578A>G , CM000666.2:g.183289578A>G	GRCh38
NC_000004.11:g.184210731A>G , CM000666.1:g.184210731A>G	GRCh37
NC_000004.10:g.184447725A>G	NCBI36
NG_051586.1:g.195944A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3327A>G MANE Select	ENSP00000384222.3:p.Pro1109=
ENST00000403733.7:c.3327A>G	ENSP00000384222.3:p.Pro1109=
ENST00000427431.5:c.*2719A>G	ENSP00000393342.1:n.*2719A>G
ENST00000438543.5:c.*1123A>G	ENSP00000413521.1:n.*1123A>G
ENST00000448232.6:c.3399A>G	ENSP00000398577.2:p.Pro1133=
ENST00000504005.5:c.2373A>G	ENSP00000427569.1:p.Pro791=
ENST00000508747.1:c.711A>G	ENSP00000420835.1:p.Pro237=
ENST00000513834.5:c.3180A>G	ENSP00000425054.1:p.Pro1060=
NM_024949.5:c.3327A>G	NP_079225.5:p.Pro1109=
XM_011532269.1:c.3399A>G	XP_011530571.1:p.Pro1133=
XM_011532269.3:c.3399A>G	XP_011530571.1:p.Pro1133=
XM_024454225.1:c.3105A>G	XP_024309993.1:p.Pro1035=
NM_024949.6:c.3327A>G MANE Select	NP_079225.5:p.Pro1109=