Canonical Allele Identifier: CA2688364626
Gene: CCN3 HGNC NCBI

Linked Data

gnomAD v4: 8-119423581-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.119423581G>T , CM000670.2:g.119423581G>T GRCh38
NC_000008.10:g.120435821G>T , CM000670.1:g.120435821G>T GRCh37
NC_000008.9:g.120505002G>T NCBI36
NG_009779.1:g.12270G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000259526.4:c.*449G>T MANE Select ENSP00000259526.3:n.*449G>T
ENST00000259526.3:c.*449G>T ENSP00000259526.3:n.*449G>T
NM_002514.3:c.*449G>T NP_002505.1:n.*449G>T
NM_002514.4:c.*449G>T MANE Select NP_002505.1:n.*449G>T
Search 100 bp 5'
Search 100 bp 3'