Canonical Allele Identifier: CA846366055
Gene: CCN3 HGNC NCBI

Linked Data

dbSNP Id: rs1042725526
gnomAD v4: 8-119423579-A-T
MyVariant Identifiers: chr8:g.120435819A>T (hg19) chr8:g.119423579A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.119423579A>T , CM000670.2:g.119423579A>T GRCh38
NC_000008.10:g.120435819A>T , CM000670.1:g.120435819A>T GRCh37
NC_000008.9:g.120505000A>T NCBI36
NG_009779.1:g.12268A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000259526.4:c.*447A>T MANE Select ENSP00000259526.3:n.*447A>T
ENST00000259526.3:c.*447A>T ENSP00000259526.3:n.*447A>T
NM_002514.3:c.*447A>T NP_002505.1:n.*447A>T
NM_002514.4:c.*447A>T MANE Select NP_002505.1:n.*447A>T
Search 100 bp 5'
Search 100 bp 3'