Canonical Allele Identifier: CA569670406

Gene: CCN6

Linked Data

• dbSNP Id: rs1554314834
• gnomAD v2: 6-112390874-A-C
• gnomAD v3: 6-112069671-A-C
• gnomAD v4: 6-112069671-A-C
• MyVariant Identifiers: chr6:g.112390874A>C (hg19) ; chr6:g.112069671A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069671A>C , CM000668.2:g.112069671A>C	GRCh38
NC_000006.11:g.112390874A>C , CM000668.1:g.112390874A>C	GRCh37
NC_000006.10:g.112497567A>C	NCBI36
NG_011748.1:g.20597A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*51A>C MANE Select	ENSP00000357655.4:n.*51A>C
ENST00000639360.1:c.1017A>C	ENSP00000491774.1:n.1017A>C
ENST00000230529.9:c.*51A>C	ENSP00000230529.5:n.*51A>C
ENST00000361714.5:c.*51A>C	ENSP00000354734.2:n.*51A>C
ENST00000368666.6:c.*51A>C	ENSP00000357655.3:n.*51A>C
ENST00000454589.5:c.*520A>C	ENSP00000395928.1:n.*520A>C
ENST00000604763.5:c.*51A>C	ENSP00000473777.1:n.*51A>C
ENST00000620524.3:n.1047A>C
NM_003880.3:c.*51A>C	NP_003871.1:n.*51A>C
NM_198239.1:c.*51A>C	NP_937882.1:n.*51A>C
NR_125353.1:n.1370A>C
NR_125354.1:n.1290A>C
XM_011536220.1:c.*51A>C	XP_011534522.1:n.*51A>C
XM_011536221.1:c.*520A>C	XP_011534523.1:n.*520A>C
XM_011536223.1:c.*51A>C	XP_011534525.1:n.*51A>C
XM_011536223.3:c.*51A>C	XP_011534525.1:n.*51A>C
XR_001743705.1:n.1718A>C
NM_003880.4:c.*51A>C	NP_003871.1:n.*51A>C
NM_198239.2:c.*51A>C MANE Select	NP_937882.2:n.*51A>C
NR_125353.2:n.1434A>C
NR_125354.3:n.1261A>C