Canonical Allele Identifier: CA2680045449
Gene: CCN6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069705G>C , CM000668.2:g.112069705G>C GRCh38
NC_000006.11:g.112390908G>C , CM000668.1:g.112390908G>C GRCh37
NC_000006.10:g.112497601G>C NCBI36
NG_011748.1:g.20631G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*85G>C ENSP00000354734.2:n.*85G>C
ENST00000368666.6:c.*85G>C ENSP00000357655.3:n.*85G>C