ClinGen Allele Registry
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Canonical Allele Identifier:
CA783082788
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.9099202G>C
GRCh37
chr18:g.9099200G>C
Linked Data - Sequence & Population
gnomAD v3:
18:9099202 G / C
gnomAD v4:
chr18-9099202-G-C
Joint Max Group AF
0.00021524 (AMR)
Genomes Max Group AF
0.00021524 (AMR)
Linked Data - NCBI & NCI
dbSNP:
6506640
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.9099202G>C , CM000680.2:g.9099202G>C
GRCh38
NC_000018.9:g.9099200G>C , CM000680.1:g.9099200G>C
GRCh37
NC_000018.8:g.9089200G>C
NCBI36
NG_013355.1:g.1573G>C
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