Canonical Allele Identifier: CA1655201677
Gene: CCN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069763T= , CM000668.2:g.112069763T= GRCh38
NC_000006.11:g.112390966T= , CM000668.1:g.112390966T= GRCh37
NC_000006.10:g.112497659T= NCBI36
NG_011748.1:g.20689T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*143T= ENSP00000354734.2:n.*143T=
ENST00000368666.6:c.*143T= ENSP00000357655.3:n.*143T=