ClinGen Allele Registry
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Canonical Allele Identifier:
CA15075722
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.165717968G>A
GRCh37
chr1:g.165687205G>A
Linked Data - Sequence & Population
gnomAD v2:
1:165687205 G / A
gnomAD v3:
1:165717968 G / A
gnomAD v4:
chr1-165717968-G-A
Joint Max Group AF
0.96711654 (EAS)
Genomes Max Group AF
0.96711654 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4656461
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.165717968G>A , CM000663.2:g.165717968G>A
GRCh38
NC_000001.10:g.165687205G>A , CM000663.1:g.165687205G>A
GRCh37
NC_000001.9:g.163953829G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'