Canonical Allele Identifier: CA100241207

Gene: CCNG2

Linked Data

• dbSNP Id: rs953875870
• MyVariant Identifiers: chr4:g.77215836T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.77215836T>A , CM000666.2:g.77215836T>A	GRCh38
NC_000004.11:g.78136989T>A , CM000666.1:g.78136989T>A	GRCh37
NC_000004.10:g.78356013T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497512.5:n.1675+23569T>A
ENST00000514756.1:n.101+23569T>A