Canonical Allele Identifier: CA248428
Gene: ADAMTS9-AS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 162162
ClinVar RCV Id: RCV000190298
dbSNP Id: rs6795735
gnomAD v2: 3-64705365-C-T
gnomAD v3: 3-64719689-C-T
gnomAD v4: 3-64719689-C-T
MyVariant Identifiers: chr3:g.64705365C>T (hg19) chr3:g.64719689C>T (hg38)
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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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