Canonical Allele Identifier: CA1469917052
Gene: CCNG2 HGNC NCBI

Linked Data

dbSNP Id: rs1718768983

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215935G>C , CM000666.2:g.77215935G>C GRCh38
NC_000004.11:g.78137088G>C , CM000666.1:g.78137088G>C GRCh37
NC_000004.10:g.78356112G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000497512.5:n.1675+23668G>C
ENST00000514756.1:n.101+23668G>C