Canonical Allele Identifier: CA1469916991
Gene: CCNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215794T= , CM000666.2:g.77215794T= GRCh38
NC_000004.11:g.78136947T= , CM000666.1:g.78136947T= GRCh37
NC_000004.10:g.78355971T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000497512.5:n.1675+23527T=
ENST00000514756.1:n.101+23527T=