ClinGen Allele Registry
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Canonical Allele Identifier:
CA12465518
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.45922864T>G
GRCh37
chr7:g.45962463T>G
Linked Data - Sequence & Population
gnomAD v2:
7:45962463 T / G
gnomAD v3:
7:45922864 T / G
gnomAD v4:
chr7-45922864-T-G
Joint Max Group AF
0.87257163 (AFR)
Genomes Max Group AF
0.87257163 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2132570
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.45922864T>G , CM000669.2:g.45922864T>G
GRCh38
NC_000007.13:g.45962463T>G , CM000669.1:g.45962463T>G
GRCh37
NC_000007.12:g.45928988T>G
NCBI36
NG_011508.1:g.3409A>C
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