Canonical Allele Identifier: CA2680045442
Gene: CCN6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069696A>G , CM000668.2:g.112069696A>G GRCh38
NC_000006.11:g.112390899A>G , CM000668.1:g.112390899A>G GRCh37
NC_000006.10:g.112497592A>G NCBI36
NG_011748.1:g.20622A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*76A>G ENSP00000354734.2:n.*76A>G
ENST00000368666.6:c.*76A>G ENSP00000357655.3:n.*76A>G