Canonical Allele Identifier: CA1064386193
Gene: CCNG2 HGNC NCBI

Linked Data

dbSNP Id: rs1718767367
gnomAD v3: 4-77215803-T-A
gnomAD v4: 4-77215803-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215803T>A , CM000666.2:g.77215803T>A GRCh38
NC_000004.11:g.78136956T>A , CM000666.1:g.78136956T>A GRCh37
NC_000004.10:g.78355980T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000497512.5:n.1675+23536T>A
ENST00000514756.1:n.101+23536T>A
Search 100 bp 5'
Search 100 bp 3'