Canonical Allele Identifier: CA1814710437
Gene: CCN3 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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