Canonical Allele Identifier: CA248428
Gene: ADAMTS9-AS2 HGNC NCBI
MyVariant.info:
GRCh38 chr3:g.64719689C>T
GRCh37 chr3:g.64705365C>T
gnomAD v2:
3:64705365 C / T
gnomAD v3:
3:64719689 C / T
gnomAD v4:
chr3-64719689-C-T
Joint Max Group AF 0.81124186 (AFR)
Genomes Max Group AF 0.81124186 (AFR)
ClinVar RCV:
RCV000190298
ClinVar Variation:
162162
dbSNP:
6795735
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.64719689C>T , CM000665.2:g.64719689C>T GRCh38
NC_000003.11:g.64705365C>T , CM000665.1:g.64705365C>T GRCh37
NC_000003.10:g.64680405C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038264.1:n.469+34351C>T
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