Canonical Allele Identifier: CA324359418
Gene: CBX7 HGNC NCBI

Linked Data

dbSNP Id: rs183025300
gnomAD v2: 22-39519133-C-T
gnomAD v3: 22-39123128-C-T
gnomAD v4: 22-39123128-C-T
MyVariant Identifiers: chr22:g.39519133C>T (hg19) chr22:g.39123128C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.39123128C>T , CM000684.2:g.39123128C>T GRCh38
NC_000022.10:g.39519133C>T , CM000684.1:g.39519133C>T GRCh37
NC_000022.9:g.37849079C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000475962.5:n.45-2555G>A
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