Canonical Allele Identifier: CA2580832655
Gene: CCN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.119423572C>A , CM000670.2:g.119423572C>A GRCh38
NC_000008.10:g.120435812C>A , CM000670.1:g.120435812C>A GRCh37
NC_000008.9:g.120504993C>A NCBI36
NG_009779.1:g.12261C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000259526.4:c.*440C>A MANE Select ENSP00000259526.3:n.*440C>A
ENST00000259526.3:c.*440C>A ENSP00000259526.3:n.*440C>A
NM_002514.3:c.*440C>A NP_002505.1:n.*440C>A
NM_002514.4:c.*440C>A MANE Select NP_002505.1:n.*440C>A