Canonical Allele Identifier: CA2837686626
Gene: CCNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215771C>A , CM000666.2:g.77215771C>A GRCh38
NC_000004.11:g.78136924C>A , CM000666.1:g.78136924C>A GRCh37
NC_000004.10:g.78355948C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000497512.5:n.1675+23504C>A
ENST00000514756.1:n.101+23504C>A