Canonical Allele Identifier: CA798675395

Gene: CCNG2

Linked Data

• dbSNP Id: rs1173786614
• gnomAD v3: 4-77215716-A-G
• gnomAD v4: 4-77215716-A-G
• MyVariant Identifiers: chr4:g.78136869A>G (hg19) ; chr4:g.77215716A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.77215716A>G , CM000666.2:g.77215716A>G	GRCh38
NC_000004.11:g.78136869A>G , CM000666.1:g.78136869A>G	GRCh37
NC_000004.10:g.78355893A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497512.5:n.1675+23449A>G
ENST00000514756.1:n.101+23449A>G