Canonical Allele Identifier: CA1655201662
Gene: CCN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069724C= , CM000668.2:g.112069724C= GRCh38
NC_000006.11:g.112390927C= , CM000668.1:g.112390927C= GRCh37
NC_000006.10:g.112497620C= NCBI36
NG_011748.1:g.20650C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*104C= ENSP00000354734.2:n.*104C=
ENST00000368666.6:c.*104C= ENSP00000357655.3:n.*104C=