ClinGen Allele Registry
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Canonical Allele Identifier:
CA14045598
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.100676553G>A
GRCh37
chr14:g.101142890G>A
Linked Data - Sequence & Population
gnomAD v2:
14:101142890 G / A
gnomAD v3:
14:100676553 G / A
gnomAD v4:
chr14-100676553-G-A
Joint Max Group AF
0.85714393 (NFE)
Genomes Max Group AF
0.8571943 (NFE)
Exomes Max Group AF
0.79262679 (NFE)
Linked Data - NCBI & NCI
dbSNP:
730570
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.100676553G>A , CM000676.2:g.100676553G>A
GRCh38
NC_000014.8:g.101142890G>A , CM000676.1:g.101142890G>A
GRCh37
NC_000014.7:g.100212643G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'