ClinGen Allele Registry
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Canonical Allele Identifier:
CA11206887
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr2:g.203875952G>A
GRCh37
chr2:g.204740675G>A
Linked Data - Sequence & Population
gnomAD v2:
2:204740675 G / A
gnomAD v3:
2:203875952 G / A
gnomAD v4:
chr2-203875952-G-A
Joint Max Group AF
0.57321568 (EAS)
Genomes Max Group AF
0.57321568 (EAS)
Linked Data - NCBI & NCI
dbSNP:
231725
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.203875952G>A , CM000664.2:g.203875952G>A
GRCh38
NC_000002.11:g.204740675G>A , CM000664.1:g.204740675G>A
GRCh37
NC_000002.10:g.204448920G>A
NCBI36
NG_011502.1:g.13167G>A
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