Canonical Allele Identifier: CA100241209
Gene: CCNG2 HGNC NCBI

Linked Data

dbSNP Id: rs975543240
gnomAD v2: 4-78136995-T-C
gnomAD v3: 4-77215842-T-C
gnomAD v4: 4-77215842-T-C
MyVariant Identifiers: chr4:g.78136995T>C (hg19) chr4:g.77215842T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215842T>C , CM000666.2:g.77215842T>C GRCh38
NC_000004.11:g.78136995T>C , CM000666.1:g.78136995T>C GRCh37
NC_000004.10:g.78356019T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000497512.5:n.1675+23575T>C
ENST00000514756.1:n.101+23575T>C
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