Canonical Allele Identifier: CA10621276

Gene: CCN6

Linked Data

• ClinVar Variation Id: 355062
• ClinVar RCV Id: RCV000274318
• dbSNP Id: rs886060987
• MyVariant Identifiers: chr6:g.112382328C>T (hg19) ; chr6:g.112061125C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061125C>T , CM000668.2:g.112061125C>T	GRCh38
NC_000006.11:g.112382328C>T , CM000668.1:g.112382328C>T	GRCh37
NC_000006.10:g.112489021C>T	NCBI36
NG_011748.1:g.12051C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.183C>T MANE Select	ENSP00000357655.4:p.Cys61=
ENST00000639360.1:c.87C>T	ENSP00000491774.1:p.Cys29=
ENST00000230529.9:c.183C>T	ENSP00000230529.5:p.Cys61=
ENST00000361714.5:c.183C>T	ENSP00000354734.2:p.Cys61=
ENST00000368663.4:c.183C>T	ENSP00000357652.4:p.Cys61=
ENST00000368664.7:c.237C>T	ENSP00000357653.3:p.Cys79=
ENST00000368666.6:c.237C>T	ENSP00000357655.3:p.Cys79=
ENST00000409166.5:c.-507-154C>T	ENSP00000386467.1:n.-507-154C>T
ENST00000454589.5:c.183C>T	ENSP00000395928.1:p.Cys61=
ENST00000604763.5:c.183C>T	ENSP00000473777.1:p.Cys61=
ENST00000620524.3:n.117C>T
NM_003880.3:c.183C>T	NP_003871.1:p.Cys61=
NM_198239.1:c.237C>T	NP_937882.1:p.Cys79=
NR_125353.1:n.373C>T
NR_125354.1:n.293C>T
XM_011536220.1:c.183C>T	XP_011534522.1:p.Cys61=
XM_011536221.1:c.246C>T	XP_011534523.1:p.Cys82=
XM_011536222.1:c.321C>T	XP_011534524.1:p.Cys107=
XM_011536222.2:c.246C>T	XP_011534524.2:p.Cys82=
XR_001743705.1:n.721C>T
NM_003880.4:c.183C>T	NP_003871.1:p.Cys61=
NM_198239.2:c.183C>T MANE Select	NP_937882.2:p.Cys61=
NR_125353.2:n.437C>T
NR_125354.3:n.264C>T