Canonical Allele Identifier: CA817273923
Gene: CCN6 HGNC NCBI

Linked Data

dbSNP Id: rs1266455604
gnomAD v3: 6-112069718-T-C
gnomAD v4: 6-112069718-T-C
MyVariant Identifiers: chr6:g.112069718T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

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