Canonical Allele Identifier: CA792055383

Gene: WWC2

Linked Data

• dbSNP Id: rs1312695606
• MyVariant Identifiers: chr4:g.184210952T>C (hg19) ; chr4:g.183289799T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289799T>C , CM000666.2:g.183289799T>C	GRCh38
NC_000004.11:g.184210952T>C , CM000666.1:g.184210952T>C	GRCh37
NC_000004.10:g.184447946T>C	NCBI36
NG_051586.1:g.196165T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3384+164T>C MANE Select	ENSP00000384222.3:n.3384+164T>C
ENST00000403733.7:c.3384+164T>C	ENSP00000384222.3:n.3384+164T>C
ENST00000427431.5:c.*2776+164T>C	ENSP00000393342.1:n.*2776+164T>C
ENST00000438543.5:c.*1180+164T>C	ENSP00000413521.1:n.*1180+164T>C
ENST00000448232.6:c.3456+164T>C	ENSP00000398577.2:n.3456+164T>C
ENST00000504005.5:c.2430+164T>C	ENSP00000427569.1:n.2430+164T>C
ENST00000508747.1:c.768+164T>C	ENSP00000420835.1:n.768+164T>C
ENST00000513834.5:c.3237+164T>C	ENSP00000425054.1:n.3237+164T>C
NM_024949.5:c.3384+164T>C	NP_079225.5:n.3384+164T>C
XM_011532269.1:c.3456+164T>C	XP_011530571.1:n.3456+164T>C
XM_011532269.3:c.3456+164T>C	XP_011530571.1:n.3456+164T>C
XM_024454225.1:c.3162+164T>C	XP_024309993.1:n.3162+164T>C
NM_024949.6:c.3384+164T>C MANE Select	NP_079225.5:n.3384+164T>C