ClinGen Allele Registry
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Canonical Allele Identifier:
CA15948567
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr19:g.29245435G>A
GRCh37
chr19:g.29736342G>A
Linked Data - Sequence & Population
gnomAD v2:
19:29736342 G / A
gnomAD v3:
19:29245435 G / A
gnomAD v4:
chr19-29245435-G-A
Joint Max Group AF
0.44859108 (EAS)
Genomes Max Group AF
0.44859108 (EAS)
Linked Data - NCBI & NCI
dbSNP:
11083866
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.29245435G>A , CM000681.2:g.29245435G>A
GRCh38
NC_000019.9:g.29736342G>A , CM000681.1:g.29736342G>A
GRCh37
NC_000019.8:g.34428182G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'