ClinGen Allele Registry
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Canonical Allele Identifier:
CA12228296
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.24646593C>T
GRCh37
chr6:g.24646821C>T
Linked Data - Sequence & Population
gnomAD v2:
6:24646821 C / T
gnomAD v3:
6:24646593 C / T
gnomAD v4:
chr6-24646593-C-T
Joint Max Group AF
0.45744573 (AFR)
Genomes Max Group AF
0.45744573 (AFR)
Linked Data - NCBI & NCI
dbSNP:
3756821
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.24646593C>T , CM000668.2:g.24646593C>T
GRCh38
NC_000006.11:g.24646821C>T , CM000668.1:g.24646821C>T
GRCh37
NC_000006.10:g.24754800C>T
NCBI36
NG_016206.1:g.4563G>A
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