Canonical Allele Identifier: CA1655201649
Gene: CCN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069690T= , CM000668.2:g.112069690T= GRCh38
NC_000006.11:g.112390893T= , CM000668.1:g.112390893T= GRCh37
NC_000006.10:g.112497586T= NCBI36
NG_011748.1:g.20616T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*70T= ENSP00000354734.2:n.*70T=
ENST00000368666.6:c.*70T= ENSP00000357655.3:n.*70T=