Canonical Allele Identifier: CA184959577
Gene: CCN3 HGNC NCBI

Linked Data

dbSNP Id: rs1010424225
MyVariant Identifiers: chr8:g.120435816G>A (hg19) chr8:g.119423576G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.119423576G>A , CM000670.2:g.119423576G>A GRCh38
NC_000008.10:g.120435816G>A , CM000670.1:g.120435816G>A GRCh37
NC_000008.9:g.120504997G>A NCBI36
NG_009779.1:g.12265G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000259526.4:c.*444G>A MANE Select ENSP00000259526.3:n.*444G>A
ENST00000259526.3:c.*444G>A ENSP00000259526.3:n.*444G>A
NM_002514.3:c.*444G>A NP_002505.1:n.*444G>A
NM_002514.4:c.*444G>A MANE Select NP_002505.1:n.*444G>A
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