Canonical Allele Identifier: CA817273956
Gene: CCN6 HGNC NCBI

Linked Data

dbSNP Id: rs1222146385
gnomAD v4: 6-112069760-C-CTTT
MyVariant Identifiers: chr6:g.112069760_112069761insTTT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069762_112069764dup , CM000668.2:g.112069762_112069764dup GRCh38
NC_000006.11:g.112390965_112390967dup , CM000668.1:g.112390965_112390967dup GRCh37
NC_000006.10:g.112497658_112497660dup NCBI36
NG_011748.1:g.20688_20690dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*142_*144dup ENSP00000354734.2:n.*142_*144dup
ENST00000368666.6:c.*142_*144dup ENSP00000357655.3:n.*142_*144dup
Search 100 bp 5'
Search 100 bp 3'