Canonical Allele Identifier: CA909332713
Gene: ADAMTS9-AS2 HGNC NCBI

Linked Data

dbSNP Id: rs6795735
MyVariant Identifiers: chr3:g.64705365C>G (hg19) chr3:g.64719689C>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
NR_038264.1:n.469+34351C>G
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