Canonical Allele Identifier: CA2688364620
Gene: CCN3 HGNC NCBI

Linked Data

gnomAD v4: 8-119423577-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.119423577G>A , CM000670.2:g.119423577G>A GRCh38
NC_000008.10:g.120435817G>A , CM000670.1:g.120435817G>A GRCh37
NC_000008.9:g.120504998G>A NCBI36
NG_009779.1:g.12266G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000259526.4:c.*445G>A MANE Select ENSP00000259526.3:n.*445G>A
ENST00000259526.3:c.*445G>A ENSP00000259526.3:n.*445G>A
NM_002514.3:c.*445G>A NP_002505.1:n.*445G>A
NM_002514.4:c.*445G>A MANE Select NP_002505.1:n.*445G>A
Search 100 bp 5'
Search 100 bp 3'