Canonical Allele Identifier: CA358846379
Gene: WWC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.183289609A>G , CM000666.2:g.183289609A>G GRCh38
NC_000004.11:g.184210762A>G , CM000666.1:g.184210762A>G GRCh37
NC_000004.10:g.184447756A>G NCBI36
NG_051586.1:g.195975A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000403733.8:c.3358A>G MANE Select ENSP00000384222.3:p.Arg1120Gly
ENST00000403733.7:c.3358A>G ENSP00000384222.3:p.Arg1120Gly
ENST00000427431.5:c.*2750A>G ENSP00000393342.1:n.*2750A>G
ENST00000438543.5:c.*1154A>G ENSP00000413521.1:n.*1154A>G
ENST00000448232.6:c.3430A>G ENSP00000398577.2:p.Arg1144Gly
ENST00000504005.5:c.2404A>G ENSP00000427569.1:p.Arg802Gly
ENST00000508747.1:c.742A>G ENSP00000420835.1:p.Arg248Gly
ENST00000513834.5:c.3211A>G ENSP00000425054.1:p.Arg1071Gly
NM_024949.5:c.3358A>G NP_079225.5:p.Arg1120Gly
XM_011532269.1:c.3430A>G XP_011530571.1:p.Arg1144Gly
XM_011532269.3:c.3430A>G XP_011530571.1:p.Arg1144Gly
XM_024454225.1:c.3136A>G XP_024309993.1:p.Arg1046Gly
NM_024949.6:c.3358A>G MANE Select NP_079225.5:p.Arg1120Gly