Canonical Allele Identifier: CA100241205

Gene: CCNG2

Linked Data

• dbSNP Id: rs1017289008
• gnomAD v2: 4-78136963-A-C
• gnomAD v3: 4-77215810-A-C
• gnomAD v4: 4-77215810-A-C
• MyVariant Identifiers: chr4:g.78136963A>C (hg19) ; chr4:g.77215810A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.77215810A>C , CM000666.2:g.77215810A>C	GRCh38
NC_000004.11:g.78136963A>C , CM000666.1:g.78136963A>C	GRCh37
NC_000004.10:g.78355987A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000497512.5:n.1675+23543A>C
ENST00000514756.1:n.101+23543A>C