ClinGen Allele Registry
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Canonical Allele Identifier:
CA303407567
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.75795614T>A
GRCh37
chr18:g.73507569T>A
Linked Data - Sequence & Population
gnomAD v3:
18:75795614 T / A
gnomAD v4:
chr18-75795614-T-A
Joint Max Group AF
0.00000488 (NFE)
Genomes Max Group AF
0.00000488 (NFE)
Linked Data - NCBI & NCI
dbSNP:
12326088
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.75795614T>A , CM000680.2:g.75795614T>A
GRCh38
NC_000018.9:g.73507569T>A , CM000680.1:g.73507569T>A
GRCh37
NC_000018.8:g.71636557T>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'