Canonical Allele Identifier: CA1814710436
Gene: CCN3 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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