Canonical Allele Identifier: CA569670409

Gene: CCN6

Linked Data

• dbSNP Id: rs1554314850
• gnomAD v2: 6-112390930-A-C
• gnomAD v3: 6-112069727-A-C
• gnomAD v4: 6-112069727-A-C
• MyVariant Identifiers: chr6:g.112390930A>C (hg19) ; chr6:g.112069727A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069727A>C , CM000668.2:g.112069727A>C	GRCh38
NC_000006.11:g.112390930A>C , CM000668.1:g.112390930A>C	GRCh37
NC_000006.10:g.112497623A>C	NCBI36
NG_011748.1:g.20653A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361714.5:c.*107A>C	ENSP00000354734.2:n.*107A>C
ENST00000368666.6:c.*107A>C	ENSP00000357655.3:n.*107A>C