Canonical Allele Identifier: CA817273911
Gene: CCN6 HGNC NCBI

Linked Data

dbSNP Id: rs1468595534
MyVariant Identifiers: chr6:g.112069700A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069700A>G , CM000668.2:g.112069700A>G GRCh38
NC_000006.11:g.112390903A>G , CM000668.1:g.112390903A>G GRCh37
NC_000006.10:g.112497596A>G NCBI36
NG_011748.1:g.20626A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*80A>G ENSP00000354734.2:n.*80A>G
ENST00000368666.6:c.*80A>G ENSP00000357655.3:n.*80A>G