Canonical Allele Identifier: CA358845795

Gene: WWC2

Linked Data

• dbSNP Id: rs1487477505
• gnomAD v2: 4-184210591-G-A
• MyVariant Identifiers: chr4:g.184210591G>A (hg19) ; chr4:g.183289438G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289438G>A , CM000666.2:g.183289438G>A	GRCh38
NC_000004.11:g.184210591G>A , CM000666.1:g.184210591G>A	GRCh37
NC_000004.10:g.184447585G>A	NCBI36
NG_051586.1:g.195804G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3187G>A MANE Select	ENSP00000384222.3:p.Val1063Met
ENST00000403733.7:c.3187G>A	ENSP00000384222.3:p.Val1063Met
ENST00000427431.5:c.*2579G>A	ENSP00000393342.1:n.*2579G>A
ENST00000438543.5:c.*983G>A	ENSP00000413521.1:n.*983G>A
ENST00000448232.6:c.3259G>A	ENSP00000398577.2:p.Val1087Met
ENST00000504005.5:c.2233G>A	ENSP00000427569.1:p.Val745Met
ENST00000508747.1:c.571G>A	ENSP00000420835.1:p.Val191Met
ENST00000513834.5:c.3040G>A	ENSP00000425054.1:p.Val1014Met
NM_024949.5:c.3187G>A	NP_079225.5:p.Val1063Met
XM_011532269.1:c.3259G>A	XP_011530571.1:p.Val1087Met
XM_011532269.3:c.3259G>A	XP_011530571.1:p.Val1087Met
XM_024454225.1:c.2965G>A	XP_024309993.1:p.Val989Met
NM_024949.6:c.3187G>A MANE Select	NP_079225.5:p.Val1063Met