Canonical Allele Identifier: CA798675411
Gene: CCNG2 HGNC NCBI

Linked Data

dbSNP Id: rs1213173896
gnomAD v3: 4-77215751-T-A
gnomAD v4: 4-77215751-T-A
MyVariant Identifiers: chr4:g.78136904T>A (hg19) chr4:g.77215751T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215751T>A , CM000666.2:g.77215751T>A GRCh38
NC_000004.11:g.78136904T>A , CM000666.1:g.78136904T>A GRCh37
NC_000004.10:g.78355928T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000497512.5:n.1675+23484T>A
ENST00000514756.1:n.101+23484T>A
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