Canonical Allele Identifier: CA3964153

Gene: CCN6

Linked Data

• dbSNP Id: rs782583394
• ExAC: 6:112390843 A / C
• gnomAD v2: 6-112390843-A-C
• gnomAD v4: 6-112069640-A-C
• MyVariant Identifiers: chr6:g.112390843A>C (hg19) ; chr6:g.112069640A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069640A>C , CM000668.2:g.112069640A>C	GRCh38
NC_000006.11:g.112390843A>C , CM000668.1:g.112390843A>C	GRCh37
NC_000006.10:g.112497536A>C	NCBI36
NG_011748.1:g.20566A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*20A>C MANE Select	ENSP00000357655.4:n.*20A>C
ENST00000639360.1:c.986A>C	ENSP00000491774.1:n.986A>C
ENST00000230529.9:c.*20A>C	ENSP00000230529.5:n.*20A>C
ENST00000361714.5:c.*20A>C	ENSP00000354734.2:n.*20A>C
ENST00000368663.4:c.*391A>C	ENSP00000357652.4:n.*391A>C
ENST00000368664.7:c.*489A>C	ENSP00000357653.3:n.*489A>C
ENST00000368666.6:c.*20A>C	ENSP00000357655.3:n.*20A>C
ENST00000409166.5:c.*20A>C	ENSP00000386467.1:n.*20A>C
ENST00000454589.5:c.*489A>C	ENSP00000395928.1:n.*489A>C
ENST00000604763.5:c.*20A>C	ENSP00000473777.1:n.*20A>C
ENST00000613648.1:n.920A>C
ENST00000620524.3:n.1016A>C
NM_003880.3:c.*20A>C	NP_003871.1:n.*20A>C
NM_198239.1:c.*20A>C	NP_937882.1:n.*20A>C
NR_125353.1:n.1339A>C
NR_125354.1:n.1259A>C
XM_011536220.1:c.*20A>C	XP_011534522.1:n.*20A>C
XM_011536221.1:c.*489A>C	XP_011534523.1:n.*489A>C
XM_011536223.1:c.*20A>C	XP_011534525.1:n.*20A>C
XM_011536223.3:c.*20A>C	XP_011534525.1:n.*20A>C
XR_001743705.1:n.1687A>C
NM_003880.4:c.*20A>C	NP_003871.1:n.*20A>C
NM_198239.2:c.*20A>C MANE Select	NP_937882.2:n.*20A>C
NR_125353.2:n.1403A>C
NR_125354.3:n.1230A>C