Canonical Allele Identifier: CA792054659

Gene: WWC2

Linked Data

• dbSNP Id: rs1335658877
• gnomAD v3: 4-183289316-C-T
• gnomAD v4: 4-183289316-C-T
• MyVariant Identifiers: chr4:g.184210469C>T (hg19) ; chr4:g.183289316C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289316C>T , CM000666.2:g.183289316C>T	GRCh38
NC_000004.11:g.184210469C>T , CM000666.1:g.184210469C>T	GRCh37
NC_000004.10:g.184447463C>T	NCBI36
NG_051586.1:g.195682C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3142-77C>T MANE Select	ENSP00000384222.3:n.3142-77C>T
ENST00000403733.7:c.3142-77C>T	ENSP00000384222.3:n.3142-77C>T
ENST00000427431.5:c.*2534-77C>T	ENSP00000393342.1:n.*2534-77C>T
ENST00000438543.5:c.*938-77C>T	ENSP00000413521.1:n.*938-77C>T
ENST00000448232.6:c.3214-77C>T	ENSP00000398577.2:n.3214-77C>T
ENST00000504005.5:c.2188-77C>T	ENSP00000427569.1:n.2188-77C>T
ENST00000508747.1:c.526-77C>T	ENSP00000420835.1:n.526-77C>T
ENST00000513834.5:c.2995-77C>T	ENSP00000425054.1:n.2995-77C>T
NM_024949.5:c.3142-77C>T	NP_079225.5:n.3142-77C>T
XM_011532269.1:c.3214-77C>T	XP_011530571.1:n.3214-77C>T
XM_011532269.3:c.3214-77C>T	XP_011530571.1:n.3214-77C>T
XM_024454225.1:c.2920-77C>T	XP_024309993.1:n.2920-77C>T
NM_024949.6:c.3142-77C>T MANE Select	NP_079225.5:n.3142-77C>T