ClinGen Allele Registry
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Canonical Allele Identifier:
CA11340981
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr2:g.143932550C>T
GRCh37
chr2:g.144690117C>T
Linked Data - Sequence & Population
gnomAD v2:
2:144690117 C / T
gnomAD v3:
2:143932550 C / T
gnomAD v4:
chr2-143932550-C-T
Joint Max Group AF
0.83851927 (NFE)
Genomes Max Group AF
0.83851927 (NFE)
Linked Data - NCBI & NCI
dbSNP:
1011397
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.143932550C>T , CM000664.2:g.143932550C>T
GRCh38
NC_000002.11:g.144690117C>T , CM000664.1:g.144690117C>T
GRCh37
NC_000002.10:g.144406587C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'