Canonical Allele Identifier: CA3150320

Gene: WWC2

Linked Data

• dbSNP Id: rs763000869
• ExAC: 4:184210698 G / A
• gnomAD v2: 4-184210698-G-A
• gnomAD v4: 4-183289545-G-A
• MyVariant Identifiers: chr4:g.184210698G>A (hg19) ; chr4:g.183289545G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289545G>A , CM000666.2:g.183289545G>A	GRCh38
NC_000004.11:g.184210698G>A , CM000666.1:g.184210698G>A	GRCh37
NC_000004.10:g.184447692G>A	NCBI36
NG_051586.1:g.195911G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3294G>A MANE Select	ENSP00000384222.3:p.Glu1098=
ENST00000403733.7:c.3294G>A	ENSP00000384222.3:p.Glu1098=
ENST00000427431.5:c.*2686G>A	ENSP00000393342.1:n.*2686G>A
ENST00000438543.5:c.*1090G>A	ENSP00000413521.1:n.*1090G>A
ENST00000448232.6:c.3366G>A	ENSP00000398577.2:p.Glu1122=
ENST00000504005.5:c.2340G>A	ENSP00000427569.1:p.Glu780=
ENST00000508747.1:c.678G>A	ENSP00000420835.1:p.Glu226=
ENST00000513834.5:c.3147G>A	ENSP00000425054.1:p.Glu1049=
NM_024949.5:c.3294G>A	NP_079225.5:p.Glu1098=
XM_011532269.1:c.3366G>A	XP_011530571.1:p.Glu1122=
XM_011532269.3:c.3366G>A	XP_011530571.1:p.Glu1122=
XM_024454225.1:c.3072G>A	XP_024309993.1:p.Glu1024=
NM_024949.6:c.3294G>A MANE Select	NP_079225.5:p.Glu1098=