ClinGen Allele Registry
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Canonical Allele Identifier:
CA909332715
Gene: ADAMTS9-AS2
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.64719689C>A
GRCh37
chr3:g.64705365C>A
Linked Data - NCBI & NCI
dbSNP:
6795735
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.64719689C>A , CM000665.2:g.64719689C>A
GRCh38
NC_000003.11:g.64705365C>A , CM000665.1:g.64705365C>A
GRCh37
NC_000003.10:g.64680405C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_038264.1:n.469+34351C>A
Search 100 bp 5'
Search 100 bp 3'