Canonical Allele Identifier: CA798675535
Gene: CCNG2 HGNC NCBI

Linked Data

dbSNP Id: rs1167744616
gnomAD v3: 4-77215940-C-G
gnomAD v4: 4-77215940-C-G
MyVariant Identifiers: chr4:g.78137093C>G (hg19) chr4:g.77215940C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215940C>G , CM000666.2:g.77215940C>G GRCh38
NC_000004.11:g.78137093C>G , CM000666.1:g.78137093C>G GRCh37
NC_000004.10:g.78356117C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000497512.5:n.1675+23673C>G
ENST00000514756.1:n.101+23673C>G
Search 100 bp 5'
Search 100 bp 3'