ClinGen Allele Registry
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Canonical Allele Identifier:
CA14600338
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.11282320G>A
GRCh37
chr18:g.11282319G>A
Linked Data - Sequence & Population
gnomAD v2:
18:11282319 G / A
gnomAD v3:
18:11282320 G / A
gnomAD v4:
chr18-11282320-G-A
Joint Max Group AF
0.8287366 (NFE)
Genomes Max Group AF
0.8287366 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7243066
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.11282320G>A , CM000680.2:g.11282320G>A
GRCh38
NC_000018.9:g.11282319G>A , CM000680.1:g.11282319G>A
GRCh37
NC_000018.8:g.11272319G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'