Canonical Allele Identifier: CA3150311

Gene: WWC2

Linked Data

• dbSNP Id: rs149738870
• ExAC: 4:184210655 A / G
• gnomAD v2: 4-184210655-A-G
• gnomAD v3: 4-183289502-A-G
• gnomAD v4: 4-183289502-A-G
• MyVariant Identifiers: chr4:g.184210655A>G (hg19) ; chr4:g.183289502A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289502A>G , CM000666.2:g.183289502A>G	GRCh38
NC_000004.11:g.184210655A>G , CM000666.1:g.184210655A>G	GRCh37
NC_000004.10:g.184447649A>G	NCBI36
NG_051586.1:g.195868A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3251A>G MANE Select	ENSP00000384222.3:p.Asn1084Ser
ENST00000403733.7:c.3251A>G	ENSP00000384222.3:p.Asn1084Ser
ENST00000427431.5:c.*2643A>G	ENSP00000393342.1:n.*2643A>G
ENST00000438543.5:c.*1047A>G	ENSP00000413521.1:n.*1047A>G
ENST00000448232.6:c.3323A>G	ENSP00000398577.2:p.Asn1108Ser
ENST00000504005.5:c.2297A>G	ENSP00000427569.1:p.Asn766Ser
ENST00000508747.1:c.635A>G	ENSP00000420835.1:p.Asn212Ser
ENST00000513834.5:c.3104A>G	ENSP00000425054.1:p.Asn1035Ser
NM_024949.5:c.3251A>G	NP_079225.5:p.Asn1084Ser
XM_011532269.1:c.3323A>G	XP_011530571.1:p.Asn1108Ser
XM_011532269.3:c.3323A>G	XP_011530571.1:p.Asn1108Ser
XM_024454225.1:c.3029A>G	XP_024309993.1:p.Asn1010Ser
NM_024949.6:c.3251A>G MANE Select	NP_079225.5:p.Asn1084Ser