Canonical Allele Identifier: CA2680045445
Gene: CCN6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069699T>G , CM000668.2:g.112069699T>G GRCh38
NC_000006.11:g.112390902T>G , CM000668.1:g.112390902T>G GRCh37
NC_000006.10:g.112497595T>G NCBI36
NG_011748.1:g.20625T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*79T>G ENSP00000354734.2:n.*79T>G
ENST00000368666.6:c.*79T>G ENSP00000357655.3:n.*79T>G