Canonical Allele Identifier: CA100241216
Gene: CCNG2 HGNC NCBI

Linked Data

dbSNP Id: rs746821521
MyVariant Identifiers: chr4:g.78137038A>G (hg19) chr4:g.77215885A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215885A>G , CM000666.2:g.77215885A>G GRCh38
NC_000004.11:g.78137038A>G , CM000666.1:g.78137038A>G GRCh37
NC_000004.10:g.78356062A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000497512.5:n.1675+23618A>G
ENST00000514756.1:n.101+23618A>G
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