Canonical Allele Identifier: CA1655201679
Gene: CCN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069765A= , CM000668.2:g.112069765A= GRCh38
NC_000006.11:g.112390968A= , CM000668.1:g.112390968A= GRCh37
NC_000006.10:g.112497661A= NCBI36
NG_011748.1:g.20691A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*145A= ENSP00000354734.2:n.*145A=
ENST00000368666.6:c.*145A= ENSP00000357655.3:n.*145A=