ClinGen Allele Registry
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Canonical Allele Identifier:
CA63790190
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.203874161C>G
GRCh37
chr2:g.204738884C>G
Linked Data - Sequence & Population
gnomAD v2:
2:204738884 C / G
gnomAD v3:
2:203874161 C / G
gnomAD v4:
chr2-203874161-C-G
Joint Max Group AF
0.00104636 (EAS)
Genomes Max Group AF
0.00104636 (EAS)
Linked Data - NCBI & NCI
dbSNP:
139354616
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.203874161C>G , CM000664.2:g.203874161C>G
GRCh38
NC_000002.11:g.204738884C>G , CM000664.1:g.204738884C>G
GRCh37
NC_000002.10:g.204447129C>G
NCBI36
NG_011502.1:g.11376C>G
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