Canonical Allele Identifier: CA1518546779
Gene: WWC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.183289644C= , CM000666.2:g.183289644C= GRCh38
NC_000004.11:g.184210797C= , CM000666.1:g.184210797C= GRCh37
NC_000004.10:g.184447791C= NCBI36
NG_051586.1:g.196010C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403733.8:c.3384+9C= MANE Select ENSP00000384222.3:n.3384+9C=
ENST00000403733.7:c.3384+9C= ENSP00000384222.3:n.3384+9C=
ENST00000427431.5:c.*2776+9C= ENSP00000393342.1:n.*2776+9C=
ENST00000438543.5:c.*1180+9C= ENSP00000413521.1:n.*1180+9C=
ENST00000448232.6:c.3456+9C= ENSP00000398577.2:n.3456+9C=
ENST00000504005.5:c.2430+9C= ENSP00000427569.1:n.2430+9C=
ENST00000508747.1:c.768+9C= ENSP00000420835.1:n.768+9C=
ENST00000513834.5:c.3237+9C= ENSP00000425054.1:n.3237+9C=
NM_024949.5:c.3384+9C= NP_079225.5:n.3384+9C=
XM_011532269.1:c.3456+9C= XP_011530571.1:n.3456+9C=
XM_011532269.3:c.3456+9C= XP_011530571.1:n.3456+9C=
XM_024454225.1:c.3162+9C= XP_024309993.1:n.3162+9C=
NM_024949.6:c.3384+9C= MANE Select NP_079225.5:n.3384+9C=