Canonical Allele Identifier: CA14423806
Gene:
MyVariant.info:
GRCh38 chr17:g.63476833T>A
GRCh37 chr17:g.61554194T>A
gnomAD v2:
17:61554194 T / A
gnomAD v3:
17:63476833 T / A
gnomAD v4:
chr17-63476833-T-A
Joint Max Group AF 0.6671984 (AMR)
Genomes Max Group AF 0.6671984 (AMR)
ClinVar RCV:
RCV001610167
ClinVar Variation:
1231511
dbSNP:
4291
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.63476833T>A , CM000679.2:g.63476833T>A GRCh38
NC_000017.10:g.61554194T>A , CM000679.1:g.61554194T>A GRCh37
NC_000017.9:g.58907926T>A NCBI36
NG_011648.1:g.4761T>A
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