Canonical Allele Identifier: CA1093230486
Gene: CCN6 HGNC NCBI

Linked Data

dbSNP Id: rs1776820263

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069738A>G , CM000668.2:g.112069738A>G GRCh38
NC_000006.11:g.112390941A>G , CM000668.1:g.112390941A>G GRCh37
NC_000006.10:g.112497634A>G NCBI36
NG_011748.1:g.20664A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*118A>G ENSP00000354734.2:n.*118A>G
ENST00000368666.6:c.*118A>G ENSP00000357655.3:n.*118A>G