Canonical Allele Identifier: CA100241206

Gene: CCNG2

Linked Data

• dbSNP Id: rs544281549
• gnomAD v3: 4-77215831-T-C
• gnomAD v4: 4-77215831-T-C
• MyVariant Identifiers: chr4:g.78136984T>C (hg19) ; chr4:g.77215831T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.77215831T>C , CM000666.2:g.77215831T>C	GRCh38
NC_000004.11:g.78136984T>C , CM000666.1:g.78136984T>C	GRCh37
NC_000004.10:g.78356008T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497512.5:n.1675+23564T>C
ENST00000514756.1:n.101+23564T>C