Canonical Allele Identifier: CA442557686

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210722T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289569T>C , CM000666.2:g.183289569T>C	GRCh38
NC_000004.11:g.184210722T>C , CM000666.1:g.184210722T>C	GRCh37
NC_000004.10:g.184447716T>C	NCBI36
NG_051586.1:g.195935T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3318T>C MANE Select	ENSP00000384222.3:p.Thr1106=
ENST00000403733.7:c.3318T>C	ENSP00000384222.3:p.Thr1106=
ENST00000427431.5:c.*2710T>C	ENSP00000393342.1:n.*2710T>C
ENST00000438543.5:c.*1114T>C	ENSP00000413521.1:n.*1114T>C
ENST00000448232.6:c.3390T>C	ENSP00000398577.2:p.Thr1130=
ENST00000504005.5:c.2364T>C	ENSP00000427569.1:p.Thr788=
ENST00000508747.1:c.702T>C	ENSP00000420835.1:p.Thr234=
ENST00000513834.5:c.3171T>C	ENSP00000425054.1:p.Thr1057=
NM_024949.5:c.3318T>C	NP_079225.5:p.Thr1106=
XM_011532269.1:c.3390T>C	XP_011530571.1:p.Thr1130=
XM_011532269.3:c.3390T>C	XP_011530571.1:p.Thr1130=
XM_024454225.1:c.3096T>C	XP_024309993.1:p.Thr1032=
NM_024949.6:c.3318T>C MANE Select	NP_079225.5:p.Thr1106=