ClinGen Allele Registry
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Canonical Allele Identifier:
CA11042336
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.203706103G>A
GRCh37
chr2:g.204570826G>A
Linked Data - Sequence & Population
gnomAD v2:
2:204570826 G / A
gnomAD v3:
2:203706103 G / A
gnomAD v4:
chr2-203706103-G-A
Joint Max Group AF
0.58590729 (SAS)
Genomes Max Group AF
0.58590729 (SAS)
Linked Data - NCBI & NCI
dbSNP:
35593994
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.203706103G>A , CM000664.2:g.203706103G>A
GRCh38
NC_000002.11:g.204570826G>A , CM000664.1:g.204570826G>A
GRCh37
NC_000002.10:g.204279071G>A
NCBI36
NG_029618.1:g.4629G>A
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