ClinGen Allele Registry
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Canonical Allele Identifier:
CA753061818
Gene: CBX7
HGNC
NCBI
Linked Data
dbSNP Id:
rs1188449409
gnomAD v3:
22-39123236-G-A
gnomAD v4:
22-39123236-G-A
MyVariant Identifiers:
chr22:g.39519241G>A (hg19)
chr22:g.39123236G>A (hg38)
JSON-LD
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
Search 100 bp 5'
Search 100 bp 3'