Canonical Allele Identifier: CA1655201651
Gene: CCN6 HGNC NCBI

Linked Data

dbSNP Id: rs1776819516
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069692G>T , CM000668.2:g.112069692G>T GRCh38
NC_000006.11:g.112390895G>T , CM000668.1:g.112390895G>T GRCh37
NC_000006.10:g.112497588G>T NCBI36
NG_011748.1:g.20618G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*72G>T ENSP00000354734.2:n.*72G>T
ENST00000368666.6:c.*72G>T ENSP00000357655.3:n.*72G>T
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