Canonical Allele Identifier: CA1025685209
Gene: CBX7 HGNC NCBI

Linked Data

dbSNP Id: rs1601548143

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.39123129A>G , CM000684.2:g.39123129A>G GRCh38
NC_000022.10:g.39519134A>G , CM000684.1:g.39519134A>G GRCh37
NC_000022.9:g.37849080A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000475962.5:n.45-2556T>C