ClinGen Allele Registry
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Canonical Allele Identifier:
CA11042335
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.203705369C>T
GRCh37
chr2:g.204570092C>T
Linked Data - Sequence & Population
gnomAD v2:
2:204570092 C / T
gnomAD v3:
2:203705369 C / T
gnomAD v4:
chr2-203705369-C-T
Joint Max Group AF
0.58661291 (SAS)
Genomes Max Group AF
0.58661291 (SAS)
Linked Data - NCBI & NCI
dbSNP:
3181096
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.203705369C>T , CM000664.2:g.203705369C>T
GRCh38
NC_000002.11:g.204570092C>T , CM000664.1:g.204570092C>T
GRCh37
NC_000002.10:g.204278337C>T
NCBI36
NG_029618.1:g.3895C>T
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