Canonical Allele Identifier: CA2680045441
Gene: CCN6 HGNC NCBI

Linked Data

gnomAD v4: 6-112069695-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069695A>T , CM000668.2:g.112069695A>T GRCh38
NC_000006.11:g.112390898A>T , CM000668.1:g.112390898A>T GRCh37
NC_000006.10:g.112497591A>T NCBI36
NG_011748.1:g.20621A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*75A>T ENSP00000354734.2:n.*75A>T
ENST00000368666.6:c.*75A>T ENSP00000357655.3:n.*75A>T
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