Canonical Allele Identifier: CA15614050
Gene:
MyVariant.info:
GRCh38 chr9:g.5260079C>T
GRCh37 chr9:g.5260079C>T
gnomAD v2:
9:5260079 C / T
gnomAD v3:
9:5260079 C / T
gnomAD v4:
chr9-5260079-C-T
Joint Max Group AF 0.60682967 (AFR)
Genomes Max Group AF 0.60682967 (AFR)
dbSNP:
1830610
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.5260079C>T , CM000671.2:g.5260079C>T GRCh38
NC_000009.11:g.5260079C>T , CM000671.1:g.5260079C>T GRCh37
NC_000009.10:g.5250079C>T NCBI36
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