Canonical Allele Identifier: CA753061785
Gene: CBX7 HGNC NCBI

Linked Data

dbSNP Id: rs139371

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.39123191T>G , CM000684.2:g.39123191T>G GRCh38
NC_000022.10:g.39519196T>G , CM000684.1:g.39519196T>G GRCh37
NC_000022.9:g.37849142T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475962.5:n.45-2618A>C