ClinGen Allele Registry
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Canonical Allele Identifier:
CA14067733
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.41233395G>A
GRCh37
chr14:g.41702598G>A
Linked Data - Sequence & Population
gnomAD v2:
14:41702598 G / A
gnomAD v3:
14:41233395 G / A
gnomAD v4:
chr14-41233395-G-A
Joint Max Group AF
0.31622447 (AMR)
Genomes Max Group AF
0.31622447 (AMR)
Linked Data - NCBI & NCI
dbSNP:
1612141
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.41233395G>A , CM000676.2:g.41233395G>A
GRCh38
NC_000014.8:g.41702598G>A , CM000676.1:g.41702598G>A
GRCh37
NC_000014.7:g.40772348G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'