Canonical Allele Identifier: CA365369474

Gene: CCN6

Linked Data

• dbSNP Id: rs1776509826
• gnomAD v4: 6-112061186-C-T
• MyVariant Identifiers: chr6:g.112382389C>T (hg19) ; chr6:g.112061186C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061186C>T , CM000668.2:g.112061186C>T	GRCh38
NC_000006.11:g.112382389C>T , CM000668.1:g.112382389C>T	GRCh37
NC_000006.10:g.112489082C>T	NCBI36
NG_011748.1:g.12112C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.244C>T MANE Select	ENSP00000357655.4:p.Pro82Ser
ENST00000639360.1:c.148C>T	ENSP00000491774.1:p.Pro50Ser
ENST00000230529.9:c.244C>T	ENSP00000230529.5:p.Pro82Ser
ENST00000361714.5:c.244C>T	ENSP00000354734.2:p.Pro82Ser
ENST00000368663.4:c.244C>T	ENSP00000357652.4:p.Pro82Ser
ENST00000368664.7:c.298C>T	ENSP00000357653.3:p.Pro100Ser
ENST00000368666.6:c.298C>T	ENSP00000357655.3:p.Pro100Ser
ENST00000409166.5:c.-507-93C>T	ENSP00000386467.1:n.-507-93C>T
ENST00000454589.5:c.244C>T	ENSP00000395928.1:p.Pro82Ser
ENST00000604763.5:c.244C>T	ENSP00000473777.1:p.Pro82Ser
ENST00000620524.3:n.178C>T
NM_003880.3:c.244C>T	NP_003871.1:p.Pro82Ser
NM_198239.1:c.298C>T	NP_937882.1:p.Pro100Ser
NR_125353.1:n.434C>T
NR_125354.1:n.354C>T
XM_011536220.1:c.244C>T	XP_011534522.1:p.Pro82Ser
XM_011536221.1:c.307C>T	XP_011534523.1:p.Pro103Ser
XM_011536222.1:c.382C>T	XP_011534524.1:p.Pro128Ser
XM_011536222.2:c.307C>T	XP_011534524.2:p.Pro103Ser
XR_001743705.1:n.782C>T
NM_003880.4:c.244C>T	NP_003871.1:p.Pro82Ser
NM_198239.2:c.244C>T MANE Select	NP_937882.2:p.Pro82Ser
NR_125353.2:n.498C>T
NR_125354.3:n.325C>T