ClinGen Allele Registry
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Canonical Allele Identifier:
CA532938185
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.55781769T>G
GRCh37
chr2:g.56008904T>G
Linked Data - Sequence & Population
gnomAD v2:
2:56008904 T / G
gnomAD v3:
2:55781769 T / G
gnomAD v4:
chr2-55781769-T-G
Joint Max Group AF
0.00026256 (EAS)
Genomes Max Group AF
0.00026256 (EAS)
Linked Data - NCBI & NCI
dbSNP:
7577894
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.55781769T>G , CM000664.2:g.55781769T>G
GRCh38
NC_000002.11:g.56008904T>G , CM000664.1:g.56008904T>G
GRCh37
NC_000002.10:g.55862408T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'