Canonical Allele Identifier: CA100241189
Gene: CCNG2 HGNC NCBI

Linked Data

dbSNP Id: rs908625415
gnomAD v2: 4-78136842-T-A
gnomAD v3: 4-77215689-T-A
gnomAD v4: 4-77215689-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215689T>A , CM000666.2:g.77215689T>A GRCh38
NC_000004.11:g.78136842T>A , CM000666.1:g.78136842T>A GRCh37
NC_000004.10:g.78355866T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000497512.5:n.1675+23422T>A
ENST00000514756.1:n.101+23422T>A