Canonical Allele Identifier: CA798675437
Gene: CCNG2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215780G>C , CM000666.2:g.77215780G>C GRCh38
NC_000004.11:g.78136933G>C , CM000666.1:g.78136933G>C GRCh37
NC_000004.10:g.78355957G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000497512.5:n.1675+23513G>C
ENST00000514756.1:n.101+23513G>C
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