Canonical Allele Identifier: CA569670408
Gene: CCN6 HGNC NCBI

Linked Data

dbSNP Id: rs1270961440
gnomAD v2: 6-112390904-CTTTG-C
gnomAD v3: 6-112069701-CTTTG-C
gnomAD v4: 6-112069701-CTTTG-C
MyVariant Identifiers: chr6:g.112390905_112390908del (hg19) chr6:g.112069702_112069705del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069705_112069708del , CM000668.2:g.112069705_112069708del GRCh38
NC_000006.11:g.112390908_112390911del , CM000668.1:g.112390908_112390911del GRCh37
NC_000006.10:g.112497601_112497604del NCBI36
NG_011748.1:g.20631_20634del

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*85_*88del ENSP00000354734.2:n.*85_*88del
ENST00000368666.6:c.*85_*88del ENSP00000357655.3:n.*85_*88del
Search 100 bp 5'
Search 100 bp 3'