Canonical Allele Identifier: CA1655201622

Gene: CCN6

Linked Data

• dbSNP Id: rs1554314820

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069638A>C , CM000668.2:g.112069638A>C	GRCh38
NC_000006.11:g.112390841A>C , CM000668.1:g.112390841A>C	GRCh37
NC_000006.10:g.112497534A>C	NCBI36
NG_011748.1:g.20564A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*18A>C MANE Select	ENSP00000357655.4:n.*18A>C
ENST00000639360.1:c.984A>C	ENSP00000491774.1:n.984A>C
ENST00000230529.9:c.*18A>C	ENSP00000230529.5:n.*18A>C
ENST00000361714.5:c.*18A>C	ENSP00000354734.2:n.*18A>C
ENST00000368663.4:c.*389A>C	ENSP00000357652.4:n.*389A>C
ENST00000368664.7:c.*487A>C	ENSP00000357653.3:n.*487A>C
ENST00000368666.6:c.*18A>C	ENSP00000357655.3:n.*18A>C
ENST00000409166.5:c.*18A>C	ENSP00000386467.1:n.*18A>C
ENST00000454589.5:c.*487A>C	ENSP00000395928.1:n.*487A>C
ENST00000604763.5:c.*18A>C	ENSP00000473777.1:n.*18A>C
ENST00000613648.1:n.918A>C
ENST00000620524.3:n.1014A>C
NM_003880.3:c.*18A>C	NP_003871.1:n.*18A>C
NM_198239.1:c.*18A>C	NP_937882.1:n.*18A>C
NR_125353.1:n.1337A>C
NR_125354.1:n.1257A>C
XM_011536220.1:c.*18A>C	XP_011534522.1:n.*18A>C
XM_011536221.1:c.*487A>C	XP_011534523.1:n.*487A>C
XM_011536223.1:c.*18A>C	XP_011534525.1:n.*18A>C
XM_011536223.3:c.*18A>C	XP_011534525.1:n.*18A>C
XR_001743705.1:n.1685A>C
NM_003880.4:c.*18A>C	NP_003871.1:n.*18A>C
NM_198239.2:c.*18A>C MANE Select	NP_937882.2:n.*18A>C
NR_125353.2:n.1401A>C
NR_125354.3:n.1228A>C