ClinGen Allele Registry
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Canonical Allele Identifier:
CA14154768
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.74741059A>G
GRCh37
chr15:g.75033400A>G
Linked Data - Sequence & Population
gnomAD v2:
15:75033400 A / G
gnomAD v3:
15:74741059 A / G
gnomAD v4:
chr15-74741059-A-G
Joint Max Group AF
0.70665865 (NFE)
Genomes Max Group AF
0.70665865 (NFE)
Linked Data - NCBI & NCI
dbSNP:
2472299
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.74741059A>G , CM000677.2:g.74741059A>G
GRCh38
NC_000015.9:g.75033400A>G , CM000677.1:g.75033400A>G
GRCh37
NC_000015.8:g.72820453A>G
NCBI36
NG_008431.1:g.23518A>G
NG_008431.2:g.23518A>G
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