Canonical Allele Identifier: CA358846324

Gene: WWC2

Linked Data

• dbSNP Id: rs1448857276
• gnomAD v2: 4-184210736-G-C
• gnomAD v4: 4-183289583-G-C
• MyVariant Identifiers: chr4:g.184210736G>C (hg19) ; chr4:g.183289583G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289583G>C , CM000666.2:g.183289583G>C	GRCh38
NC_000004.11:g.184210736G>C , CM000666.1:g.184210736G>C	GRCh37
NC_000004.10:g.184447730G>C	NCBI36
NG_051586.1:g.195949G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3332G>C MANE Select	ENSP00000384222.3:p.Gly1111Ala
ENST00000403733.7:c.3332G>C	ENSP00000384222.3:p.Gly1111Ala
ENST00000427431.5:c.*2724G>C	ENSP00000393342.1:n.*2724G>C
ENST00000438543.5:c.*1128G>C	ENSP00000413521.1:n.*1128G>C
ENST00000448232.6:c.3404G>C	ENSP00000398577.2:p.Gly1135Ala
ENST00000504005.5:c.2378G>C	ENSP00000427569.1:p.Gly793Ala
ENST00000508747.1:c.716G>C	ENSP00000420835.1:p.Gly239Ala
ENST00000513834.5:c.3185G>C	ENSP00000425054.1:p.Gly1062Ala
NM_024949.5:c.3332G>C	NP_079225.5:p.Gly1111Ala
XM_011532269.1:c.3404G>C	XP_011530571.1:p.Gly1135Ala
XM_011532269.3:c.3404G>C	XP_011530571.1:p.Gly1135Ala
XM_024454225.1:c.3110G>C	XP_024309993.1:p.Gly1037Ala
NM_024949.6:c.3332G>C MANE Select	NP_079225.5:p.Gly1111Ala