ClinGen Allele Registry
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Canonical Allele Identifier:
CA10833222
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.18629964G>A
GRCh37
chr1:g.18956458G>A
Linked Data - Sequence & Population
gnomAD v2:
1:18956458 G / A
gnomAD v3:
1:18629964 G / A
gnomAD v4:
chr1-18629964-G-A
Joint Max Group AF
0.77329537 (AFR)
Genomes Max Group AF
0.77329537 (AFR)
Linked Data - NCBI & NCI
dbSNP:
766325
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.18629964G>A , CM000663.2:g.18629964G>A
GRCh38
NC_000001.10:g.18956458G>A , CM000663.1:g.18956458G>A
GRCh37
NC_000001.9:g.18829045G>A
NCBI36
NG_023262.1:g.3959G>A
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