Canonical Allele Identifier: CA817273933

Gene: CCN6

Linked Data

• dbSNP Id: rs1218259889
• MyVariant Identifiers: chr6:g.112069736T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069736T>C , CM000668.2:g.112069736T>C	GRCh38
NC_000006.11:g.112390939T>C , CM000668.1:g.112390939T>C	GRCh37
NC_000006.10:g.112497632T>C	NCBI36
NG_011748.1:g.20662T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361714.5:c.*116T>C	ENSP00000354734.2:n.*116T>C
ENST00000368666.6:c.*116T>C	ENSP00000357655.3:n.*116T>C