Canonical Allele Identifier: CA3150313

Gene: WWC2

Linked Data

• dbSNP Id: rs144648112
• ExAC: 4:184210670 C / T
• gnomAD v2: 4-184210670-C-T
• gnomAD v3: 4-183289517-C-T
• gnomAD v4: 4-183289517-C-T
• MyVariant Identifiers: chr4:g.184210670C>T (hg19) ; chr4:g.183289517C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289517C>T , CM000666.2:g.183289517C>T	GRCh38
NC_000004.11:g.184210670C>T , CM000666.1:g.184210670C>T	GRCh37
NC_000004.10:g.184447664C>T	NCBI36
NG_051586.1:g.195883C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3266C>T MANE Select	ENSP00000384222.3:p.Ala1089Val
ENST00000403733.7:c.3266C>T	ENSP00000384222.3:p.Ala1089Val
ENST00000427431.5:c.*2658C>T	ENSP00000393342.1:n.*2658C>T
ENST00000438543.5:c.*1062C>T	ENSP00000413521.1:n.*1062C>T
ENST00000448232.6:c.3338C>T	ENSP00000398577.2:p.Ala1113Val
ENST00000504005.5:c.2312C>T	ENSP00000427569.1:p.Ala771Val
ENST00000508747.1:c.650C>T	ENSP00000420835.1:p.Ala217Val
ENST00000513834.5:c.3119C>T	ENSP00000425054.1:p.Ala1040Val
NM_024949.5:c.3266C>T	NP_079225.5:p.Ala1089Val
XM_011532269.1:c.3338C>T	XP_011530571.1:p.Ala1113Val
XM_011532269.3:c.3338C>T	XP_011530571.1:p.Ala1113Val
XM_024454225.1:c.3044C>T	XP_024309993.1:p.Ala1015Val
NM_024949.6:c.3266C>T MANE Select	NP_079225.5:p.Ala1089Val