ClinGen Allele Registry
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Canonical Allele Identifier:
CA10915945
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.237940201C>T
GRCh37
chr1:g.238103501C>T
Linked Data - Sequence & Population
gnomAD v2:
1:238103501 C / T
gnomAD v3:
1:237940201 C / T
gnomAD v4:
chr1-237940201-C-T
Joint Max Group AF
0.69336633 (AFR)
Genomes Max Group AF
0.69336633 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2499604
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.237940201C>T , CM000663.2:g.237940201C>T
GRCh38
NC_000001.10:g.238103501C>T , CM000663.1:g.238103501C>T
GRCh37
NC_000001.9:g.236170124C>T
NCBI36
NG_008799.2:g.902800C>T
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