Canonical Allele Identifier: CA2680045459
Gene: CCN6 HGNC NCBI

Linked Data

gnomAD v4: 6-112069726-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069726T>A , CM000668.2:g.112069726T>A GRCh38
NC_000006.11:g.112390929T>A , CM000668.1:g.112390929T>A GRCh37
NC_000006.10:g.112497622T>A NCBI36
NG_011748.1:g.20652T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*106T>A ENSP00000354734.2:n.*106T>A
ENST00000368666.6:c.*106T>A ENSP00000357655.3:n.*106T>A
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