Canonical Allele Identifier: CA2688364632
Gene: CCN3 HGNC NCBI

Linked Data

gnomAD v4: 8-119423585-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.119423585C>A , CM000670.2:g.119423585C>A GRCh38
NC_000008.10:g.120435825C>A , CM000670.1:g.120435825C>A GRCh37
NC_000008.9:g.120505006C>A NCBI36
NG_009779.1:g.12274C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000259526.4:c.*453C>A MANE Select ENSP00000259526.3:n.*453C>A
ENST00000259526.3:c.*453C>A ENSP00000259526.3:n.*453C>A
NM_002514.3:c.*453C>A NP_002505.1:n.*453C>A
NM_002514.4:c.*453C>A MANE Select NP_002505.1:n.*453C>A
Search 100 bp 5'
Search 100 bp 3'