Canonical Allele Identifier: CA1655201661
Gene: CCN6 HGNC NCBI

Linked Data

dbSNP Id: rs1776819898
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069723G>A , CM000668.2:g.112069723G>A GRCh38
NC_000006.11:g.112390926G>A , CM000668.1:g.112390926G>A GRCh37
NC_000006.10:g.112497619G>A NCBI36
NG_011748.1:g.20649G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*103G>A ENSP00000354734.2:n.*103G>A
ENST00000368666.6:c.*103G>A ENSP00000357655.3:n.*103G>A
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