Canonical Allele Identifier: CA1469916955
Gene: CCNG2 HGNC NCBI

Linked Data

dbSNP Id: rs1718766238

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215710C>G , CM000666.2:g.77215710C>G GRCh38
NC_000004.11:g.78136863C>G , CM000666.1:g.78136863C>G GRCh37
NC_000004.10:g.78355887C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000497512.5:n.1675+23443C>G
ENST00000514756.1:n.101+23443C>G