Canonical Allele Identifier: CA798675450

Gene: CCNG2

Linked Data

• dbSNP Id: rs1313382938
• gnomAD v3: 4-77215788-G-A
• gnomAD v4: 4-77215788-G-A
• MyVariant Identifiers: chr4:g.78136941G>A (hg19) ; chr4:g.77215788G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.77215788G>A , CM000666.2:g.77215788G>A	GRCh38
NC_000004.11:g.78136941G>A , CM000666.1:g.78136941G>A	GRCh37
NC_000004.10:g.78355965G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497512.5:n.1675+23521G>A
ENST00000514756.1:n.101+23521G>A