Canonical Allele Identifier: CA1469916996
Gene: CCNG2 HGNC NCBI

Linked Data

dbSNP Id: rs1718767330
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215802G>T , CM000666.2:g.77215802G>T GRCh38
NC_000004.11:g.78136955G>T , CM000666.1:g.78136955G>T GRCh37
NC_000004.10:g.78355979G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000497512.5:n.1675+23535G>T
ENST00000514756.1:n.101+23535G>T
Search 100 bp 5'
Search 100 bp 3'