ClinGen Allele Registry
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Canonical Allele Identifier:
CA14560861
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.45971047C>T
GRCh37
chr18:g.43551013C>T
Linked Data - Sequence & Population
gnomAD v2:
18:43551013 C / T
gnomAD v3:
18:45971047 C / T
gnomAD v4:
chr18-45971047-C-T
Joint Max Group AF
0.38703326 (AFR)
Genomes Max Group AF
0.38703326 (AFR)
Linked Data - NCBI & NCI
dbSNP:
8098701
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.45971047C>T , CM000680.2:g.45971047C>T
GRCh38
NC_000018.9:g.43551013C>T , CM000680.1:g.43551013C>T
GRCh37
NC_000018.8:g.41805011C>T
NCBI36
NG_042838.1:g.1293G>A
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