ClinGen Allele Registry
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Canonical Allele Identifier:
CA14114348
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.22832212A>G
GRCh37
chr15:g.23040856T>C
Linked Data - Sequence & Population
gnomAD v2:
15:23040856 T / C
gnomAD v3:
15:22832212 A / G
gnomAD v4:
chr15-22832212-A-G
Joint Max Group AF
0.87855795 (EAS)
Genomes Max Group AF
0.87855795 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4778334
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.22832212A>G , CM000677.2:g.22832212A>G
GRCh38
NC_000015.9:g.23040856T>C , CM000677.1:g.23040856T>C
GRCh37
NC_000015.8:g.20592297T>C
NCBI36
Search 100 bp 5'
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