ClinGen Allele Registry
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Canonical Allele Identifier:
CA13944746
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.82911659T>G
GRCh37
chr14:g.83378003T>G
Linked Data - Sequence & Population
gnomAD v2:
14:83378003 T / G
gnomAD v3:
14:82911659 T / G
gnomAD v4:
chr14-82911659-T-G
Joint Max Group AF
0.21507068 (AMR)
Genomes Max Group AF
0.21507068 (AMR)
Linked Data - NCBI & NCI
dbSNP:
12050412
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.82911659T>G , CM000676.2:g.82911659T>G
GRCh38
NC_000014.8:g.83378003T>G , CM000676.1:g.83378003T>G
GRCh37
NC_000014.7:g.82447756T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'