Canonical Allele Identifier: CA817273918
Gene: CCN6 HGNC NCBI

Linked Data

dbSNP Id: rs1490130836
gnomAD v3: 6-112069705-G-A
gnomAD v4: 6-112069705-G-A
MyVariant Identifiers: chr6:g.112069705G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069705G>A , CM000668.2:g.112069705G>A GRCh38
NC_000006.11:g.112390908G>A , CM000668.1:g.112390908G>A GRCh37
NC_000006.10:g.112497601G>A NCBI36
NG_011748.1:g.20631G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*85G>A ENSP00000354734.2:n.*85G>A
ENST00000368666.6:c.*85G>A ENSP00000357655.3:n.*85G>A
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