Canonical Allele Identifier: CA144885420
Gene: CCN6 HGNC NCBI

Linked Data

dbSNP Id: rs888409648
gnomAD v3: 6-112069766-A-T
gnomAD v4: 6-112069766-A-T
MyVariant Identifiers: chr6:g.112069766A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069766A>T , CM000668.2:g.112069766A>T GRCh38
NC_000006.11:g.112390969A>T , CM000668.1:g.112390969A>T GRCh37
NC_000006.10:g.112497662A>T NCBI36
NG_011748.1:g.20692A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*146A>T ENSP00000354734.2:n.*146A>T
ENST00000368666.6:c.*146A>T ENSP00000357655.3:n.*146A>T
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