ClinGen Allele Registry
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Canonical Allele Identifier:
CA14524321
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.77173985G>A
GRCh37
chr18:g.74885941G>A
Linked Data - Sequence & Population
gnomAD v2:
18:74885941 G / A
gnomAD v3:
18:77173985 G / A
gnomAD v4:
chr18-77173985-G-A
Joint Max Group AF
0.75719511 (EAS)
Genomes Max Group AF
0.75719511 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4890912
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.77173985G>A , CM000680.2:g.77173985G>A
GRCh38
NC_000018.9:g.74885941G>A , CM000680.1:g.74885941G>A
GRCh37
NC_000018.8:g.73014929G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'