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Canonical Allele Identifier:
CA15222413
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.233595452C>T
GRCh37
chr2:g.234504098C>T
Linked Data - Sequence & Population
gnomAD v2:
2:234504098 C / T
gnomAD v3:
2:233595452 C / T
gnomAD v4:
chr2-233595452-C-T
Joint Max Group AF
0.64226832 (SAS)
Genomes Max Group AF
0.64226832 (SAS)
Linked Data - NCBI & NCI
dbSNP:
1597944
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.233595452C>T , CM000664.2:g.233595452C>T
GRCh38
NC_000002.11:g.234504098C>T , CM000664.1:g.234504098C>T
GRCh37
NC_000002.10:g.234168837C>T
NCBI36
NG_002601.2:g.10709C>T
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