ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
CA15280323
Gene: ADAMTS9-AS2
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr3:g.64726228C>T
GRCh37
chr3:g.64711904C>T
Linked Data - Sequence & Population
gnomAD v2:
3:64711904 C / T
gnomAD v3:
3:64726228 C / T
gnomAD v4:
chr3-64726228-C-T
Joint Max Group AF
0.50297087 (SAS)
Genomes Max Group AF
0.50297087 (SAS)
Linked Data - NCBI & NCI
dbSNP:
4607103
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.64726228C>T , CM000665.2:g.64726228C>T
GRCh38
NC_000003.11:g.64711904C>T , CM000665.1:g.64711904C>T
GRCh37
NC_000003.10:g.64686944C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_038264.1:n.469+40890C>T
Search 100 bp 5'
Search 100 bp 3'