Canonical Allele Identifier: CA569670410

Gene: CCN6

Linked Data

• dbSNP Id: rs1554314853
• gnomAD v2: 6-112390938-A-C
• gnomAD v3: 6-112069735-A-C
• gnomAD v4: 6-112069735-A-C
• MyVariant Identifiers: chr6:g.112390938A>C (hg19) ; chr6:g.112069735A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069735A>C , CM000668.2:g.112069735A>C	GRCh38
NC_000006.11:g.112390938A>C , CM000668.1:g.112390938A>C	GRCh37
NC_000006.10:g.112497631A>C	NCBI36
NG_011748.1:g.20661A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361714.5:c.*115A>C	ENSP00000354734.2:n.*115A>C
ENST00000368666.6:c.*115A>C	ENSP00000357655.3:n.*115A>C