Canonical Allele Identifier: CA442557707

Gene: WWC2

Linked Data

• dbSNP Id: rs2111076141
• MyVariant Identifiers: chr4:g.184210749T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289596T>C , CM000666.2:g.183289596T>C	GRCh38
NC_000004.11:g.184210749T>C , CM000666.1:g.184210749T>C	GRCh37
NC_000004.10:g.184447743T>C	NCBI36
NG_051586.1:g.195962T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3345T>C MANE Select	ENSP00000384222.3:p.Asp1115=
ENST00000403733.7:c.3345T>C	ENSP00000384222.3:p.Asp1115=
ENST00000427431.5:c.*2737T>C	ENSP00000393342.1:n.*2737T>C
ENST00000438543.5:c.*1141T>C	ENSP00000413521.1:n.*1141T>C
ENST00000448232.6:c.3417T>C	ENSP00000398577.2:p.Asp1139=
ENST00000504005.5:c.2391T>C	ENSP00000427569.1:p.Asp797=
ENST00000508747.1:c.729T>C	ENSP00000420835.1:p.Asp243=
ENST00000513834.5:c.3198T>C	ENSP00000425054.1:p.Asp1066=
NM_024949.5:c.3345T>C	NP_079225.5:p.Asp1115=
XM_011532269.1:c.3417T>C	XP_011530571.1:p.Asp1139=
XM_011532269.3:c.3417T>C	XP_011530571.1:p.Asp1139=
XM_024454225.1:c.3123T>C	XP_024309993.1:p.Asp1041=
NM_024949.6:c.3345T>C MANE Select	NP_079225.5:p.Asp1115=