ClinGen Allele Registry
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Canonical Allele Identifier:
CA10690112
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr1:g.165026476G>A
GRCh37
chr1:g.164995713G>A
Linked Data - Sequence & Population
gnomAD v2:
1:164995713 G / A
gnomAD v3:
1:165026476 G / A
gnomAD v4:
chr1-165026476-G-A
Joint Max Group AF
0.6107566 (NFE)
Genomes Max Group AF
0.6107566 (NFE)
Linked Data - NCBI & NCI
dbSNP:
4387163
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.165026476G>A , CM000663.2:g.165026476G>A
GRCh38
NC_000001.10:g.164995713G>A , CM000663.1:g.164995713G>A
GRCh37
NC_000001.9:g.163262337G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'