ClinGen Allele Registry
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Canonical Allele Identifier:
CA298296852
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr18:g.31756628A>G
GRCh37
chr18:g.29336591A>G
Linked Data - Sequence & Population
gnomAD v2:
18:29336591 A / G
gnomAD v3:
18:31756628 A / G
gnomAD v4:
chr18-31756628-A-G
Joint Max Group AF
0.17525178 (AFR)
Genomes Max Group AF
0.17525178 (AFR)
Linked Data - NCBI & NCI
dbSNP:
10502575
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.31756628A>G , CM000680.2:g.31756628A>G
GRCh38
NC_000018.9:g.29336591A>G , CM000680.1:g.29336591A>G
GRCh37
NC_000018.8:g.27590589A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
XR_935338.1:n.66-5511A>G
Search 100 bp 5'
Search 100 bp 3'