Canonical Allele Identifier: CA2680045468
Gene: CCN6 HGNC NCBI

Linked Data

gnomAD v4: 6-112069740-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069740T>C , CM000668.2:g.112069740T>C GRCh38
NC_000006.11:g.112390943T>C , CM000668.1:g.112390943T>C GRCh37
NC_000006.10:g.112497636T>C NCBI36
NG_011748.1:g.20666T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*120T>C ENSP00000354734.2:n.*120T>C
ENST00000368666.6:c.*120T>C ENSP00000357655.3:n.*120T>C
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