Canonical Allele Identifier: CA2680045454
Gene: CCN6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069717A>G , CM000668.2:g.112069717A>G GRCh38
NC_000006.11:g.112390920A>G , CM000668.1:g.112390920A>G GRCh37
NC_000006.10:g.112497613A>G NCBI36
NG_011748.1:g.20643A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*97A>G ENSP00000354734.2:n.*97A>G
ENST00000368666.6:c.*97A>G ENSP00000357655.3:n.*97A>G