ClinGen Allele Registry
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Canonical Allele Identifier:
CA14667973
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr19:g.1102115G>C
GRCh37
chr19:g.1102114G>C
Linked Data - Sequence & Population
gnomAD v2:
19:1102114 G / C
gnomAD v3:
19:1102115 G / C
gnomAD v4:
chr19-1102115-G-C
Joint Max Group AF
0.58630757 (AFR)
Genomes Max Group AF
0.58630757 (AFR)
Linked Data - NCBI & NCI
dbSNP:
757229
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.1102115G>C , CM000681.2:g.1102115G>C
GRCh38
NC_000019.9:g.1102114G>C , CM000681.1:g.1102114G>C
GRCh37
NC_000019.8:g.1053114G>C
NCBI36
NG_050621.1:g.3190G>C
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