Canonical Allele Identifier: CA100241202
Gene: CCNG2 HGNC NCBI

Linked Data

dbSNP Id: rs1028218656
gnomAD v2: 4-78136947-T-C
gnomAD v3: 4-77215794-T-C
gnomAD v4: 4-77215794-T-C
MyVariant Identifiers: chr4:g.78136947T>C (hg19) chr4:g.77215794T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215794T>C , CM000666.2:g.77215794T>C GRCh38
NC_000004.11:g.78136947T>C , CM000666.1:g.78136947T>C GRCh37
NC_000004.10:g.78355971T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000497512.5:n.1675+23527T>C
ENST00000514756.1:n.101+23527T>C
Search 100 bp 5'
Search 100 bp 3'