Canonical Allele Identifier: CA798675461
Gene: CCNG2 HGNC NCBI

Linked Data

dbSNP Id: rs1472455224
MyVariant Identifiers: chr4:g.78136971A>T (hg19) chr4:g.77215818A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.77215818A>T , CM000666.2:g.77215818A>T GRCh38
NC_000004.11:g.78136971A>T , CM000666.1:g.78136971A>T GRCh37
NC_000004.10:g.78355995A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000497512.5:n.1675+23551A>T
ENST00000514756.1:n.101+23551A>T
Search 100 bp 5'
Search 100 bp 3'