Canonical Allele Identifier: CA1064386201

Gene: CCNG2

Linked Data

• dbSNP Id: rs1718767670
• gnomAD v3: 4-77215839-T-C
• gnomAD v4: 4-77215839-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.77215839T>C , CM000666.2:g.77215839T>C	GRCh38
NC_000004.11:g.78136992T>C , CM000666.1:g.78136992T>C	GRCh37
NC_000004.10:g.78356016T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000497512.5:n.1675+23572T>C
ENST00000514756.1:n.101+23572T>C