ClinGen Allele Registry
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Canonical Allele Identifier:
CA15462278
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.15664978A>T
GRCh37
chr6:g.15665209A>T
Linked Data - Sequence & Population
gnomAD v2:
6:15665209 A / T
gnomAD v3:
6:15664978 A / T
gnomAD v4:
chr6-15664978-A-T
Joint Max Group AF
0.63175093 (AFR)
Genomes Max Group AF
0.63175093 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2619538
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.15664978A>T , CM000668.2:g.15664978A>T
GRCh38
NC_000006.11:g.15665209A>T , CM000668.1:g.15665209A>T
GRCh37
NC_000006.10:g.15773188A>T
NCBI36
NG_009309.1:g.3063T>A , LRG_588:g.3063T>A
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