Canonical Allele Identifier: CA569670407

Gene: CCN6

Linked Data

• dbSNP Id: rs1554314836
• gnomAD v2: 6-112390875-T-A
• gnomAD v4: 6-112069672-T-A
• MyVariant Identifiers: chr6:g.112390875T>A (hg19) ; chr6:g.112069672T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069672T>A , CM000668.2:g.112069672T>A	GRCh38
NC_000006.11:g.112390875T>A , CM000668.1:g.112390875T>A	GRCh37
NC_000006.10:g.112497568T>A	NCBI36
NG_011748.1:g.20598T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*52T>A MANE Select	ENSP00000357655.4:n.*52T>A
ENST00000639360.1:c.1018T>A	ENSP00000491774.1:n.1018T>A
ENST00000230529.9:c.*52T>A	ENSP00000230529.5:n.*52T>A
ENST00000361714.5:c.*52T>A	ENSP00000354734.2:n.*52T>A
ENST00000368666.6:c.*52T>A	ENSP00000357655.3:n.*52T>A
ENST00000454589.5:c.*521T>A	ENSP00000395928.1:n.*521T>A
ENST00000604763.5:c.*52T>A	ENSP00000473777.1:n.*52T>A
ENST00000620524.3:n.1048T>A
NM_003880.3:c.*52T>A	NP_003871.1:n.*52T>A
NM_198239.1:c.*52T>A	NP_937882.1:n.*52T>A
NR_125353.1:n.1371T>A
NR_125354.1:n.1291T>A
XM_011536220.1:c.*52T>A	XP_011534522.1:n.*52T>A
XM_011536221.1:c.*521T>A	XP_011534523.1:n.*521T>A
XM_011536223.1:c.*52T>A	XP_011534525.1:n.*52T>A
XM_011536223.3:c.*52T>A	XP_011534525.1:n.*52T>A
XR_001743705.1:n.1719T>A
NM_003880.4:c.*52T>A	NP_003871.1:n.*52T>A
NM_198239.2:c.*52T>A MANE Select	NP_937882.2:n.*52T>A
NR_125353.2:n.1435T>A
NR_125354.3:n.1262T>A