Canonical Allele Identifier: CA753061818
Gene: CBX7 HGNC NCBI

Linked Data

dbSNP Id: rs1188449409

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.39123236G>A , CM000684.2:g.39123236G>A GRCh38
NC_000022.10:g.39519241G>A , CM000684.1:g.39519241G>A GRCh37
NC_000022.9:g.37849187G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475962.5:n.45-2663C>T