Canonical Allele Identifier: CA1093230481
Gene: CCN6 HGNC NCBI

Linked Data

dbSNP Id: rs1776820066
gnomAD v3: 6-112069734-G-C
gnomAD v4: 6-112069734-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069734G>C , CM000668.2:g.112069734G>C GRCh38
NC_000006.11:g.112390937G>C , CM000668.1:g.112390937G>C GRCh37
NC_000006.10:g.112497630G>C NCBI36
NG_011748.1:g.20660G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*114G>C ENSP00000354734.2:n.*114G>C
ENST00000368666.6:c.*114G>C ENSP00000357655.3:n.*114G>C
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