ClinGen Allele Registry
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Canonical Allele Identifier:
CA629840044
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.49001752G>A
GRCh37
chr18:g.46528122G>A
Linked Data - Sequence & Population
gnomAD v2:
18:46528122 G / A
Linked Data - NCBI & NCI
dbSNP:
1469203652
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.49001752G>A , CM000680.2:g.49001752G>A
GRCh38
NC_000018.9:g.46528122G>A , CM000680.1:g.46528122G>A
GRCh37
NC_000018.8:g.44782120G>A
NCBI36
Search 100 bp 5'
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