ClinGen Allele Registry
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Canonical Allele Identifier:
CA866872520
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr9:g.7518656T>A
GRCh37
chr9:g.7518656T>A
Linked Data - Sequence & Population
gnomAD v3:
9:7518656 T / A
gnomAD v4:
chr9-7518656-T-A
Linked Data - NCBI & NCI
dbSNP:
2381628
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.7518656T>A , CM000671.2:g.7518656T>A
GRCh38
NC_000009.11:g.7518656T>A , CM000671.1:g.7518656T>A
GRCh37
NC_000009.10:g.7508656T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'