ClinGen Allele Registry
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Canonical Allele Identifier:
CA306464919
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.24172691G>A
GRCh37
chr19:g.24355493G>A
Linked Data - Sequence & Population
gnomAD v2:
19:24355493 G / A
gnomAD v3:
19:24172691 G / A
gnomAD v4:
chr19-24172691-G-A
Joint Max Group AF
0.00037853 (AFR)
Genomes Max Group AF
0.00037853 (AFR)
Linked Data - NCBI & NCI
dbSNP:
11668609
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.24172691G>A , CM000681.2:g.24172691G>A
GRCh38
NC_000019.9:g.24355493G>A , CM000681.1:g.24355493G>A
GRCh37
NC_000019.8:g.24147333G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'