ClinGen Allele Registry
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Canonical Allele Identifier:
CA12280693
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.142446496A>G
GRCh37
chr6:g.142767633A>G
Linked Data - Sequence & Population
gnomAD v2:
6:142767633 A / G
gnomAD v3:
6:142446496 A / G
gnomAD v4:
chr6-142446496-A-G
Joint Max Group AF
0.59902987 (AFR)
Genomes Max Group AF
0.59902987 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3748069
2113357787
2113357799
2113357809
2113357845
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.142446496A>G , CM000668.2:g.142446496A>G
GRCh38
NC_000006.11:g.142767633A>G , CM000668.1:g.142767633A>G
GRCh37
NC_000006.10:g.142809326A>G
NCBI36
NG_011839.1:g.149578A>G
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