Canonical Allele Identifier: CA1655201665
Gene: CCN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069734G= , CM000668.2:g.112069734G= GRCh38
NC_000006.11:g.112390937G= , CM000668.1:g.112390937G= GRCh37
NC_000006.10:g.112497630G= NCBI36
NG_011748.1:g.20660G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*114G= ENSP00000354734.2:n.*114G=
ENST00000368666.6:c.*114G= ENSP00000357655.3:n.*114G=