Canonical Allele Identifier: CA2600600500

Gene: CCNG2

Linked Data

• dbSNP Id: rs2109953811
• gnomAD v3: 4-77215742-C-T
• gnomAD v4: 4-77215742-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.77215742C>T , CM000666.2:g.77215742C>T	GRCh38
NC_000004.11:g.78136895C>T , CM000666.1:g.78136895C>T	GRCh37
NC_000004.10:g.78355919C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497512.5:n.1675+23475C>T
ENST00000514756.1:n.101+23475C>T