Canonical Allele Identifier: CA2680045448
Gene: CCN6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069704T>C , CM000668.2:g.112069704T>C GRCh38
NC_000006.11:g.112390907T>C , CM000668.1:g.112390907T>C GRCh37
NC_000006.10:g.112497600T>C NCBI36
NG_011748.1:g.20630T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*84T>C ENSP00000354734.2:n.*84T>C
ENST00000368666.6:c.*84T>C ENSP00000357655.3:n.*84T>C