Canonical Allele Identifier: CA2680045470
Gene: CCN6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069743A>C , CM000668.2:g.112069743A>C GRCh38
NC_000006.11:g.112390946A>C , CM000668.1:g.112390946A>C GRCh37
NC_000006.10:g.112497639A>C NCBI36
NG_011748.1:g.20669A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*123A>C ENSP00000354734.2:n.*123A>C
ENST00000368666.6:c.*123A>C ENSP00000357655.3:n.*123A>C