Canonical Allele Identifier: CA2688364628
Gene: CCN3 HGNC NCBI

Linked Data

gnomAD v4: 8-119423582-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.119423582A>C , CM000670.2:g.119423582A>C GRCh38
NC_000008.10:g.120435822A>C , CM000670.1:g.120435822A>C GRCh37
NC_000008.9:g.120505003A>C NCBI36
NG_009779.1:g.12271A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000259526.4:c.*450A>C MANE Select ENSP00000259526.3:n.*450A>C
ENST00000259526.3:c.*450A>C ENSP00000259526.3:n.*450A>C
NM_002514.3:c.*450A>C NP_002505.1:n.*450A>C
NM_002514.4:c.*450A>C MANE Select NP_002505.1:n.*450A>C
Search 100 bp 5'
Search 100 bp 3'