Canonical Allele Identifier: CA2680045455
Gene: CCN6 HGNC NCBI

Linked Data

gnomAD v4: 6-112069718-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069718T>A , CM000668.2:g.112069718T>A GRCh38
NC_000006.11:g.112390921T>A , CM000668.1:g.112390921T>A GRCh37
NC_000006.10:g.112497614T>A NCBI36
NG_011748.1:g.20644T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*98T>A ENSP00000354734.2:n.*98T>A
ENST00000368666.6:c.*98T>A ENSP00000357655.3:n.*98T>A
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