Canonical Allele Identifier: CA15327100

Gene: WWC2

Linked Data

• dbSNP Id: rs955748
• gnomAD v2: 4-184215675-A-G
• gnomAD v3: 4-183294522-A-G
• gnomAD v4: 4-183294522-A-G
• MyVariant Identifiers: chr4:g.184215675A>G (hg19) ; chr4:g.183294522A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183294522A>G , CM000666.2:g.183294522A>G	GRCh38
NC_000004.11:g.184215675A>G , CM000666.1:g.184215675A>G	GRCh37
NC_000004.10:g.184452669A>G	NCBI36
NG_051586.1:g.200888A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403733.8:c.3384+4887A>G MANE Select	ENSP00000384222.3:n.3384+4887A>G
ENST00000403733.7:c.3384+4887A>G	ENSP00000384222.3:n.3384+4887A>G
ENST00000427431.5:c.*2776+4887A>G	ENSP00000393342.1:n.*2776+4887A>G
ENST00000438543.5:c.*1180+4887A>G	ENSP00000413521.1:n.*1180+4887A>G
ENST00000448232.6:c.3456+4887A>G	ENSP00000398577.2:n.3456+4887A>G
ENST00000504005.5:c.2430+4887A>G	ENSP00000427569.1:n.2430+4887A>G
ENST00000508747.1:c.768+4887A>G	ENSP00000420835.1:n.768+4887A>G
ENST00000513834.5:c.3237+4887A>G	ENSP00000425054.1:n.3237+4887A>G
NM_024949.5:c.3384+4887A>G	NP_079225.5:n.3384+4887A>G
XM_011532269.1:c.3456+4887A>G	XP_011530571.1:n.3456+4887A>G
XM_011532269.3:c.3456+4887A>G	XP_011530571.1:n.3456+4887A>G
XM_024454225.1:c.3162+4887A>G	XP_024309993.1:n.3162+4887A>G
NM_024949.6:c.3384+4887A>G MANE Select	NP_079225.5:n.3384+4887A>G