Canonical Allele Identifier: CA1469917004
Gene: CCNG2 HGNC NCBI

Linked Data

dbSNP Id: rs1718767544

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215824G>T , CM000666.2:g.77215824G>T GRCh38
NC_000004.11:g.78136977G>T , CM000666.1:g.78136977G>T GRCh37
NC_000004.10:g.78356001G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000497512.5:n.1675+23557G>T
ENST00000514756.1:n.101+23557G>T