Canonical Allele Identifier: CA184959580
Gene: CCN3 HGNC NCBI

Linked Data

dbSNP Id: rs904228880
gnomAD v3: 8-119423588-T-C
gnomAD v4: 8-119423588-T-C
MyVariant Identifiers: chr8:g.120435828T>C (hg19) chr8:g.119423588T>C (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000259526.4:c.*456T>C MANE Select ENSP00000259526.3:n.*456T>C
ENST00000259526.3:c.*456T>C ENSP00000259526.3:n.*456T>C
NM_002514.3:c.*456T>C NP_002505.1:n.*456T>C
NM_002514.4:c.*456T>C MANE Select NP_002505.1:n.*456T>C
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