Canonical Allele Identifier: CA100241186
Gene: CCNG2 HGNC NCBI

Linked Data

dbSNP Id: rs1045072907
gnomAD v3: 4-77215683-G-T
gnomAD v4: 4-77215683-G-T
MyVariant Identifiers: chr4:g.78136836G>T (hg19) chr4:g.77215683G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215683G>T , CM000666.2:g.77215683G>T GRCh38
NC_000004.11:g.78136836G>T , CM000666.1:g.78136836G>T GRCh37
NC_000004.10:g.78355860G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000497512.5:n.1675+23416G>T
ENST00000514756.1:n.101+23416G>T
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