Canonical Allele Identifier: CA2688364637
Gene: CCN3 HGNC NCBI

Linked Data

gnomAD v4: 8-119423588-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.119423588T>G , CM000670.2:g.119423588T>G GRCh38
NC_000008.10:g.120435828T>G , CM000670.1:g.120435828T>G GRCh37
NC_000008.9:g.120505009T>G NCBI36
NG_009779.1:g.12277T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000259526.4:c.*456T>G MANE Select ENSP00000259526.3:n.*456T>G
ENST00000259526.3:c.*456T>G ENSP00000259526.3:n.*456T>G
NM_002514.3:c.*456T>G NP_002505.1:n.*456T>G
NM_002514.4:c.*456T>G MANE Select NP_002505.1:n.*456T>G
Search 100 bp 5'
Search 100 bp 3'