ClinGen Allele Registry
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Canonical Allele Identifier:
CA136158234
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.24648227T>C
GRCh37
chr6:g.24648455T>C
Linked Data - Sequence & Population
gnomAD v2:
6:24648455 T / C
gnomAD v3:
6:24648227 T / C
gnomAD v4:
chr6-24648227-T-C
Joint Max Group AF
0.61364172 (EAS)
Genomes Max Group AF
0.61364172 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3212236
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.24648227T>C , CM000668.2:g.24648227T>C
GRCh38
NC_000006.11:g.24648455T>C , CM000668.1:g.24648455T>C
GRCh37
NC_000006.10:g.24756434T>C
NCBI36
NG_016206.1:g.2929A>G
NG_052787.1:g.23661A>G
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