Canonical Allele Identifier: CA649010212
Gene: CCNG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215795C>G , CM000666.2:g.77215795C>G GRCh38
NC_000004.11:g.78136948C>G , CM000666.1:g.78136948C>G GRCh37
NC_000004.10:g.78355972C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000497512.5:n.1675+23528C>G
ENST00000514756.1:n.101+23528C>G