Canonical Allele Identifier: CA144885419
Gene: CCN6 HGNC NCBI

Linked Data

dbSNP Id: rs1048373339
gnomAD v4: 6-112069737-C-T
MyVariant Identifiers: chr6:g.112069737C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069737C>T , CM000668.2:g.112069737C>T GRCh38
NC_000006.11:g.112390940C>T , CM000668.1:g.112390940C>T GRCh37
NC_000006.10:g.112497633C>T NCBI36
NG_011748.1:g.20663C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*117C>T ENSP00000354734.2:n.*117C>T
ENST00000368666.6:c.*117C>T ENSP00000357655.3:n.*117C>T
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