Canonical Allele Identifier: CA1469916989
Gene: CCNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215784C= , CM000666.2:g.77215784C= GRCh38
NC_000004.11:g.78136937C= , CM000666.1:g.78136937C= GRCh37
NC_000004.10:g.78355961C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000497512.5:n.1675+23517C=
ENST00000514756.1:n.101+23517C=