Canonical Allele Identifier: CA184959582
Gene: CCN3 HGNC NCBI

Linked Data

dbSNP Id: rs187308086
gnomAD v3: 8-119423589-A-G
gnomAD v4: 8-119423589-A-G
MyVariant Identifiers: chr8:g.120435829A>G (hg19) chr8:g.119423589A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.119423589A>G , CM000670.2:g.119423589A>G GRCh38
NC_000008.10:g.120435829A>G , CM000670.1:g.120435829A>G GRCh37
NC_000008.9:g.120505010A>G NCBI36
NG_009779.1:g.12278A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000259526.4:c.*457A>G MANE Select ENSP00000259526.3:n.*457A>G
ENST00000259526.3:c.*457A>G ENSP00000259526.3:n.*457A>G
NM_002514.3:c.*457A>G NP_002505.1:n.*457A>G
NM_002514.4:c.*457A>G MANE Select NP_002505.1:n.*457A>G
Search 100 bp 5'
Search 100 bp 3'