ClinGen Allele Registry
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Canonical Allele Identifier:
CA15227016
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.203705655G>A
GRCh37
chr2:g.204570378G>A
Linked Data - Sequence & Population
gnomAD v2:
2:204570378 G / A
gnomAD v3:
2:203705655 G / A
gnomAD v4:
chr2-203705655-G-A
Joint Max Group AF
0.58548194 (SAS)
Genomes Max Group AF
0.58548194 (SAS)
Linked Data - NCBI & NCI
dbSNP:
3181098
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.203705655G>A , CM000664.2:g.203705655G>A
GRCh38
NC_000002.11:g.204570378G>A , CM000664.1:g.204570378G>A
GRCh37
NC_000002.10:g.204278623G>A
NCBI36
NG_029618.1:g.4181G>A
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