Canonical Allele Identifier: CA442557544
Gene: WWC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.184210593G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.183289440G>C , CM000666.2:g.183289440G>C GRCh38
NC_000004.11:g.184210593G>C , CM000666.1:g.184210593G>C GRCh37
NC_000004.10:g.184447587G>C NCBI36
NG_051586.1:g.195806G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000403733.8:c.3189G>C MANE Select ENSP00000384222.3:p.Val1063=
ENST00000403733.7:c.3189G>C ENSP00000384222.3:p.Val1063=
ENST00000427431.5:c.*2581G>C ENSP00000393342.1:n.*2581G>C
ENST00000438543.5:c.*985G>C ENSP00000413521.1:n.*985G>C
ENST00000448232.6:c.3261G>C ENSP00000398577.2:p.Val1087=
ENST00000504005.5:c.2235G>C ENSP00000427569.1:p.Val745=
ENST00000508747.1:c.573G>C ENSP00000420835.1:p.Val191=
ENST00000513834.5:c.3042G>C ENSP00000425054.1:p.Val1014=
NM_024949.5:c.3189G>C NP_079225.5:p.Val1063=
XM_011532269.1:c.3261G>C XP_011530571.1:p.Val1087=
XM_011532269.3:c.3261G>C XP_011530571.1:p.Val1087=
XM_024454225.1:c.2967G>C XP_024309993.1:p.Val989=
NM_024949.6:c.3189G>C MANE Select NP_079225.5:p.Val1063=