ClinGen Allele Registry
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Canonical Allele Identifier:
CA258784304
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.38551301T>A
GRCh37
chr14:g.39020505T>A
Linked Data - Sequence & Population
gnomAD v2:
14:39020505 T / A
gnomAD v3:
14:38551301 T / A
gnomAD v4:
chr14-38551301-T-A
Joint Max Group AF
0.19281738 (EAS)
Genomes Max Group AF
0.19281738 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10498345
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.38551301T>A , CM000676.2:g.38551301T>A
GRCh38
NC_000014.8:g.39020505T>A , CM000676.1:g.39020505T>A
GRCh37
NC_000014.7:g.38090256T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'