Canonical Allele Identifier: CA2688364621
Gene: CCN3 HGNC NCBI

Linked Data

gnomAD v4: 8-119423577-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.119423577G>C , CM000670.2:g.119423577G>C GRCh38
NC_000008.10:g.120435817G>C , CM000670.1:g.120435817G>C GRCh37
NC_000008.9:g.120504998G>C NCBI36
NG_009779.1:g.12266G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000259526.4:c.*445G>C MANE Select ENSP00000259526.3:n.*445G>C
ENST00000259526.3:c.*445G>C ENSP00000259526.3:n.*445G>C
NM_002514.3:c.*445G>C NP_002505.1:n.*445G>C
NM_002514.4:c.*445G>C MANE Select NP_002505.1:n.*445G>C
Search 100 bp 5'
Search 100 bp 3'