Canonical Allele Identifier: CA358846344

Gene: WWC2

Linked Data

• MyVariant Identifiers: chr4:g.184210747G>C (hg19) ; chr4:g.183289594G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.183289594G>C , CM000666.2:g.183289594G>C	GRCh38
NC_000004.11:g.184210747G>C , CM000666.1:g.184210747G>C	GRCh37
NC_000004.10:g.184447741G>C	NCBI36
NG_051586.1:g.195960G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403733.8:c.3343G>C MANE Select	ENSP00000384222.3:p.Asp1115His
ENST00000403733.7:c.3343G>C	ENSP00000384222.3:p.Asp1115His
ENST00000427431.5:c.*2735G>C	ENSP00000393342.1:n.*2735G>C
ENST00000438543.5:c.*1139G>C	ENSP00000413521.1:n.*1139G>C
ENST00000448232.6:c.3415G>C	ENSP00000398577.2:p.Asp1139His
ENST00000504005.5:c.2389G>C	ENSP00000427569.1:p.Asp797His
ENST00000508747.1:c.727G>C	ENSP00000420835.1:p.Asp243His
ENST00000513834.5:c.3196G>C	ENSP00000425054.1:p.Asp1066His
NM_024949.5:c.3343G>C	NP_079225.5:p.Asp1115His
XM_011532269.1:c.3415G>C	XP_011530571.1:p.Asp1139His
XM_011532269.3:c.3415G>C	XP_011530571.1:p.Asp1139His
XM_024454225.1:c.3121G>C	XP_024309993.1:p.Asp1041His
NM_024949.6:c.3343G>C MANE Select	NP_079225.5:p.Asp1115His