Canonical Allele Identifier: CA2762273582
Gene: CCNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215782C>T , CM000666.2:g.77215782C>T GRCh38
NC_000004.11:g.78136935C>T , CM000666.1:g.78136935C>T GRCh37
NC_000004.10:g.78355959C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000497512.5:n.1675+23515C>T
ENST00000514756.1:n.101+23515C>T