ClinGen Allele Registry
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Canonical Allele Identifier:
CA12486879
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.145321424A>G
GRCh37
chr7:g.145018517A>G
Linked Data - Sequence & Population
gnomAD v2:
7:145018517 A / G
gnomAD v3:
7:145321424 A / G
gnomAD v4:
chr7-145321424-A-G
Joint Max Group AF
0.76660055 (EAS)
Genomes Max Group AF
0.76660055 (EAS)
Linked Data - NCBI & NCI
dbSNP:
996343
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.145321424A>G , CM000669.2:g.145321424A>G
GRCh38
NC_000007.13:g.145018517A>G , CM000669.1:g.145018517A>G
GRCh37
NC_000007.12:g.144649450A>G
NCBI36
Search 100 bp 5'
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