Canonical Allele Identifier: CA2578718041
Gene: CCN6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069706T>A , CM000668.2:g.112069706T>A GRCh38
NC_000006.11:g.112390909T>A , CM000668.1:g.112390909T>A GRCh37
NC_000006.10:g.112497602T>A NCBI36
NG_011748.1:g.20632T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*86T>A ENSP00000354734.2:n.*86T>A
ENST00000368666.6:c.*86T>A ENSP00000357655.3:n.*86T>A
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