Canonical Allele Identifier: CA442557687

Gene: WWC2

Linked Data

• dbSNP Id: rs1352910950
• gnomAD v2: 4-184210725-C-T
• gnomAD v4: 4-183289572-C-T
• MyVariant Identifiers: chr4:g.184210725C>T (hg19) ; chr4:g.183289572C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289572C>T , CM000666.2:g.183289572C>T	GRCh38
NC_000004.11:g.184210725C>T , CM000666.1:g.184210725C>T	GRCh37
NC_000004.10:g.184447719C>T	NCBI36
NG_051586.1:g.195938C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3321C>T MANE Select	ENSP00000384222.3:p.Asp1107=
ENST00000403733.7:c.3321C>T	ENSP00000384222.3:p.Asp1107=
ENST00000427431.5:c.*2713C>T	ENSP00000393342.1:n.*2713C>T
ENST00000438543.5:c.*1117C>T	ENSP00000413521.1:n.*1117C>T
ENST00000448232.6:c.3393C>T	ENSP00000398577.2:p.Asp1131=
ENST00000504005.5:c.2367C>T	ENSP00000427569.1:p.Asp789=
ENST00000508747.1:c.705C>T	ENSP00000420835.1:p.Asp235=
ENST00000513834.5:c.3174C>T	ENSP00000425054.1:p.Asp1058=
NM_024949.5:c.3321C>T	NP_079225.5:p.Asp1107=
XM_011532269.1:c.3393C>T	XP_011530571.1:p.Asp1131=
XM_011532269.3:c.3393C>T	XP_011530571.1:p.Asp1131=
XM_024454225.1:c.3099C>T	XP_024309993.1:p.Asp1033=
NM_024949.6:c.3321C>T MANE Select	NP_079225.5:p.Asp1107=