Canonical Allele Identifier: CA100241188
Gene: CCNG2 HGNC NCBI

Linked Data

dbSNP Id: rs140738875
gnomAD v2: 4-78136839-T-G
gnomAD v3: 4-77215686-T-G
gnomAD v4: 4-77215686-T-G
MyVariant Identifiers: chr4:g.78136839T>G (hg19) chr4:g.77215686T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215686T>G , CM000666.2:g.77215686T>G GRCh38
NC_000004.11:g.78136839T>G , CM000666.1:g.78136839T>G GRCh37
NC_000004.10:g.78355863T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000497512.5:n.1675+23419T>G
ENST00000514756.1:n.101+23419T>G
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