ClinGen Allele Registry
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Canonical Allele Identifier:
CA16553371
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.28479148T>C
GRCh37
chr18:g.26059112T>C
Linked Data - Sequence & Population
gnomAD v2:
18:26059112 T / C
gnomAD v3:
18:28479148 T / C
gnomAD v4:
chr18-28479148-T-C
Joint Max Group AF
0.56925197 (AFR)
Genomes Max Group AF
0.56925197 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4131805
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.28479148T>C , CM000680.2:g.28479148T>C
GRCh38
NC_000018.9:g.26059112T>C , CM000680.1:g.26059112T>C
GRCh37
NC_000018.8:g.24313110T>C
NCBI36
Search 100 bp 5'
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