Canonical Allele Identifier: CA1469917006
Gene: CCNG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215831T= , CM000666.2:g.77215831T= GRCh38
NC_000004.11:g.78136984T= , CM000666.1:g.78136984T= GRCh37
NC_000004.10:g.78356008T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000497512.5:n.1675+23564T=
ENST00000514756.1:n.101+23564T=