Canonical Allele Identifier: CA184959579
Gene: CCN3 HGNC NCBI

Linked Data

dbSNP Id: rs1042725526
MyVariant Identifiers: chr8:g.120435819A>G (hg19) chr8:g.119423579A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.119423579A>G , CM000670.2:g.119423579A>G GRCh38
NC_000008.10:g.120435819A>G , CM000670.1:g.120435819A>G GRCh37
NC_000008.9:g.120505000A>G NCBI36
NG_009779.1:g.12268A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000259526.4:c.*447A>G MANE Select ENSP00000259526.3:n.*447A>G
ENST00000259526.3:c.*447A>G ENSP00000259526.3:n.*447A>G
NM_002514.3:c.*447A>G NP_002505.1:n.*447A>G
NM_002514.4:c.*447A>G MANE Select NP_002505.1:n.*447A>G
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