Canonical Allele Identifier: CA442557614

Gene: WWC2

Linked Data

• dbSNP Id: rs1267376856
• gnomAD v3: 4-183289467-C-T
• gnomAD v4: 4-183289467-C-T
• MyVariant Identifiers: chr4:g.184210620C>T (hg19) ; chr4:g.183289467C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289467C>T , CM000666.2:g.183289467C>T	GRCh38
NC_000004.11:g.184210620C>T , CM000666.1:g.184210620C>T	GRCh37
NC_000004.10:g.184447614C>T	NCBI36
NG_051586.1:g.195833C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3216C>T MANE Select	ENSP00000384222.3:p.Asp1072=
ENST00000403733.7:c.3216C>T	ENSP00000384222.3:p.Asp1072=
ENST00000427431.5:c.*2608C>T	ENSP00000393342.1:n.*2608C>T
ENST00000438543.5:c.*1012C>T	ENSP00000413521.1:n.*1012C>T
ENST00000448232.6:c.3288C>T	ENSP00000398577.2:p.Asp1096=
ENST00000504005.5:c.2262C>T	ENSP00000427569.1:p.Asp754=
ENST00000508747.1:c.600C>T	ENSP00000420835.1:p.Asp200=
ENST00000513834.5:c.3069C>T	ENSP00000425054.1:p.Asp1023=
NM_024949.5:c.3216C>T	NP_079225.5:p.Asp1072=
XM_011532269.1:c.3288C>T	XP_011530571.1:p.Asp1096=
XM_011532269.3:c.3288C>T	XP_011530571.1:p.Asp1096=
XM_024454225.1:c.2994C>T	XP_024309993.1:p.Asp998=
NM_024949.6:c.3216C>T MANE Select	NP_079225.5:p.Asp1072=