Canonical Allele Identifier: CA3150305

Gene: WWC2

Linked Data

• dbSNP Id: rs199951348
• ExAC: 4:184210645 A / G
• gnomAD v2: 4-184210645-A-G
• gnomAD v3: 4-183289492-A-G
• gnomAD v4: 4-183289492-A-G
• MyVariant Identifiers: chr4:g.184210645A>G (hg19) ; chr4:g.183289492A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289492A>G , CM000666.2:g.183289492A>G	GRCh38
NC_000004.11:g.184210645A>G , CM000666.1:g.184210645A>G	GRCh37
NC_000004.10:g.184447639A>G	NCBI36
NG_051586.1:g.195858A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3241A>G MANE Select	ENSP00000384222.3:p.Ser1081Gly
ENST00000403733.7:c.3241A>G	ENSP00000384222.3:p.Ser1081Gly
ENST00000427431.5:c.*2633A>G	ENSP00000393342.1:n.*2633A>G
ENST00000438543.5:c.*1037A>G	ENSP00000413521.1:n.*1037A>G
ENST00000448232.6:c.3313A>G	ENSP00000398577.2:p.Ser1105Gly
ENST00000504005.5:c.2287A>G	ENSP00000427569.1:p.Ser763Gly
ENST00000508747.1:c.625A>G	ENSP00000420835.1:p.Ser209Gly
ENST00000513834.5:c.3094A>G	ENSP00000425054.1:p.Ser1032Gly
NM_024949.5:c.3241A>G	NP_079225.5:p.Ser1081Gly
XM_011532269.1:c.3313A>G	XP_011530571.1:p.Ser1105Gly
XM_011532269.3:c.3313A>G	XP_011530571.1:p.Ser1105Gly
XM_024454225.1:c.3019A>G	XP_024309993.1:p.Ser1007Gly
NM_024949.6:c.3241A>G MANE Select	NP_079225.5:p.Ser1081Gly