Canonical Allele Identifier: CA3964159

Gene: CCN6

Linked Data

• dbSNP Id: rs782420754
• ExAC: 6:112390864 T / C
• gnomAD v2: 6-112390864-T-C
• gnomAD v3: 6-112069661-T-C
• gnomAD v4: 6-112069661-T-C
• MyVariant Identifiers: chr6:g.112390864T>C (hg19) ; chr6:g.112069661T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069661T>C , CM000668.2:g.112069661T>C	GRCh38
NC_000006.11:g.112390864T>C , CM000668.1:g.112390864T>C	GRCh37
NC_000006.10:g.112497557T>C	NCBI36
NG_011748.1:g.20587T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*41T>C MANE Select	ENSP00000357655.4:n.*41T>C
ENST00000639360.1:c.1007T>C	ENSP00000491774.1:n.1007T>C
ENST00000230529.9:c.*41T>C	ENSP00000230529.5:n.*41T>C
ENST00000361714.5:c.*41T>C	ENSP00000354734.2:n.*41T>C
ENST00000368666.6:c.*41T>C	ENSP00000357655.3:n.*41T>C
ENST00000454589.5:c.*510T>C	ENSP00000395928.1:n.*510T>C
ENST00000604763.5:c.*41T>C	ENSP00000473777.1:n.*41T>C
ENST00000620524.3:n.1037T>C
NM_003880.3:c.*41T>C	NP_003871.1:n.*41T>C
NM_198239.1:c.*41T>C	NP_937882.1:n.*41T>C
NR_125353.1:n.1360T>C
NR_125354.1:n.1280T>C
XM_011536220.1:c.*41T>C	XP_011534522.1:n.*41T>C
XM_011536221.1:c.*510T>C	XP_011534523.1:n.*510T>C
XM_011536223.1:c.*41T>C	XP_011534525.1:n.*41T>C
XM_011536223.3:c.*41T>C	XP_011534525.1:n.*41T>C
XR_001743705.1:n.1708T>C
NM_003880.4:c.*41T>C	NP_003871.1:n.*41T>C
NM_198239.2:c.*41T>C MANE Select	NP_937882.2:n.*41T>C
NR_125353.2:n.1424T>C
NR_125354.3:n.1251T>C