Canonical Allele Identifier: CA569670411
Gene: CCN6 HGNC NCBI

Linked Data

dbSNP Id: rs1554314866
gnomAD v2: 6-112390964-T-C
gnomAD v3: 6-112069761-T-C
gnomAD v4: 6-112069761-T-C
MyVariant Identifiers: chr6:g.112390964T>C (hg19) chr6:g.112069761T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069761T>C , CM000668.2:g.112069761T>C GRCh38
NC_000006.11:g.112390964T>C , CM000668.1:g.112390964T>C GRCh37
NC_000006.10:g.112497657T>C NCBI36
NG_011748.1:g.20687T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*141T>C ENSP00000354734.2:n.*141T>C
ENST00000368666.6:c.*141T>C ENSP00000357655.3:n.*141T>C
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