Canonical Allele Identifier: CA12978834
Gene:
MyVariant.info:
GRCh38 chr9:g.4763176T>C
GRCh37 chr9:g.4763176T>C
gnomAD v2:
9:4763176 T / C
gnomAD v3:
9:4763176 T / C
gnomAD v4:
chr9-4763176-T-C
Joint Max Group AF 0.76973576 (EAS)
Genomes Max Group AF 0.76973576 (EAS)
dbSNP:
385893
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.4763176T>C , CM000671.2:g.4763176T>C GRCh38
NC_000009.11:g.4763176T>C , CM000671.1:g.4763176T>C GRCh37
NC_000009.10:g.4753176T>C NCBI36
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