Canonical Allele Identifier: CA347658
Gene:
MyVariant.info:
GRCh38 chr9:g.133635393T>C
GRCh37 chr9:g.136500515T>C
gnomAD v2:
9:136500515 T / C
gnomAD v3:
9:133635393 T / C
gnomAD v4:
chr9-133635393-T-C
Joint Max Group AF 0.82137165 (AFR)
Genomes Max Group AF 0.82137165 (AFR)
ClinVar RCV:
RCV000201837
ClinVar Variation:
217759
dbSNP:
1611115
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133635393T>C , CM000671.2:g.133635393T>C GRCh38
NC_000009.11:g.136500515T>C , CM000671.1:g.136500515T>C GRCh37
NC_000009.10:g.135490336T>C NCBI36
NG_008645.1:g.4031T>C
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