Canonical Allele Identifier: CA1469917019
Gene: CCNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215867A= , CM000666.2:g.77215867A= GRCh38
NC_000004.11:g.78137020A= , CM000666.1:g.78137020A= GRCh37
NC_000004.10:g.78356044A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000497512.5:n.1675+23600A=
ENST00000514756.1:n.101+23600A=