ClinGen Allele Registry
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Canonical Allele Identifier:
CA590401529
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.118584139T>A
GRCh37
chr9:g.121346417T>A
Linked Data - Sequence & Population
gnomAD v2:
9:121346417 T / A
gnomAD v3:
9:118584139 T / A
gnomAD v4:
chr9-118584139-T-A
Linked Data - NCBI & NCI
dbSNP:
1572299
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.118584139T>A , CM000671.2:g.118584139T>A
GRCh38
NC_000009.11:g.121346417T>A , CM000671.1:g.121346417T>A
GRCh37
NC_000009.10:g.120386238T>A
NCBI36
Search 100 bp 5'
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