ClinGen Allele Registry
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Canonical Allele Identifier:
CA34082730
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.186682744G>C
GRCh37
chr1:g.186651876G>C
Linked Data - Sequence & Population
gnomAD v2:
1:186651876 G / C
gnomAD v3:
1:186682744 G / C
gnomAD v4:
chr1-186682744-G-C
Joint Max Group AF
0.00062241 (AFR)
Genomes Max Group AF
0.00062241 (AFR)
Linked Data - NCBI & NCI
dbSNP:
12042763
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.186682744G>C , CM000663.2:g.186682744G>C
GRCh38
NC_000001.10:g.186651876G>C , CM000663.1:g.186651876G>C
GRCh37
NC_000001.9:g.184918499G>C
NCBI36
NG_028206.2:g.2684C>G
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