Canonical Allele Identifier: CA2688364643
Gene: CCN3 HGNC NCBI

Linked Data

gnomAD v4: 8-119423593-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.119423593G>A , CM000670.2:g.119423593G>A GRCh38
NC_000008.10:g.120435833G>A , CM000670.1:g.120435833G>A GRCh37
NC_000008.9:g.120505014G>A NCBI36
NG_009779.1:g.12282G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000259526.4:c.*461G>A MANE Select ENSP00000259526.3:n.*461G>A
ENST00000259526.3:c.*461G>A ENSP00000259526.3:n.*461G>A
NM_002514.3:c.*461G>A NP_002505.1:n.*461G>A
NM_002514.4:c.*461G>A MANE Select NP_002505.1:n.*461G>A
Search 100 bp 5'
Search 100 bp 3'