ClinGen Allele Registry
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Canonical Allele Identifier:
CA10702508
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.219586340C>T
GRCh37
chr1:g.219759682C>T
Linked Data - Sequence & Population
gnomAD v2:
1:219759682 C / T
gnomAD v3:
1:219586340 C / T
gnomAD v4:
chr1-219586340-C-T
Joint Max Group AF
0.62756869 (EAS)
Genomes Max Group AF
0.62756869 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4373767
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.219586340C>T , CM000663.2:g.219586340C>T
GRCh38
NC_000001.10:g.219759682C>T , CM000663.1:g.219759682C>T
GRCh37
NC_000001.9:g.217826305C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'