ClinGen Allele Registry
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Canonical Allele Identifier:
CA14105011
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.67807262G>A
GRCh37
chr15:g.68099600G>A
Linked Data - Sequence & Population
gnomAD v2:
15:68099600 G / A
gnomAD v3:
15:67807262 G / A
gnomAD v4:
chr15-67807262-G-A
Joint Max Group AF
0.57387809 (EAS)
Genomes Max Group AF
0.57585198 (EAS)
Exomes Max Group AF
0.55389874 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2278076
2140576237
2140576242
2140576253
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.67807262G>A , CM000677.2:g.67807262G>A
GRCh38
NC_000015.9:g.68099600G>A , CM000677.1:g.68099600G>A
GRCh37
NC_000015.8:g.65886654G>A
NCBI36
NG_029143.1:g.269580G>A
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