ClinGen Allele Registry
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Canonical Allele Identifier:
CA15389266
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.154489480G>A
GRCh37
chr5:g.153869040G>A
Linked Data - Sequence & Population
gnomAD v2:
5:153869040 G / A
gnomAD v3:
5:154489480 G / A
gnomAD v4:
chr5-154489480-G-A
Joint Max Group AF
0.52952656 (AFR)
Genomes Max Group AF
0.52952656 (AFR)
Linked Data - NCBI & NCI
dbSNP:
13165478
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.154489480G>A , CM000667.2:g.154489480G>A
GRCh38
NC_000005.9:g.153869040G>A , CM000667.1:g.153869040G>A
GRCh37
NC_000005.8:g.153849233G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'