Canonical Allele Identifier: CA1469917026
Gene: CCNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215879_77215880delinsAG , CM000666.2:g.77215879_77215880delinsAG GRCh38
NC_000004.11:g.78137032_78137033delinsAG , CM000666.1:g.78137032_78137033delinsAG GRCh37
NC_000004.10:g.78356056_78356057delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000497512.5:n.1675+23612_1675+23613delinsAG
ENST00000514756.1:n.101+23612_101+23613delinsAG