Canonical Allele Identifier: CA1469916994
Gene: CCNG2 HGNC NCBI

Linked Data

dbSNP Id: rs1718767304

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215801G>A , CM000666.2:g.77215801G>A GRCh38
NC_000004.11:g.78136954G>A , CM000666.1:g.78136954G>A GRCh37
NC_000004.10:g.78355978G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000497512.5:n.1675+23534G>A
ENST00000514756.1:n.101+23534G>A