ClinGen Allele Registry
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Canonical Allele Identifier:
CA14084639
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr15:g.67542218T>C
GRCh37
chr15:g.67834556T>C
Linked Data - Sequence & Population
gnomAD v2:
15:67834556 T / C
gnomAD v3:
15:67542218 T / C
gnomAD v4:
chr15-67542218-T-C
Joint Max Group AF
0.77286658 (NFE)
Genomes Max Group AF
0.77284896 (NFE)
Exomes Max Group AF
0.46952186 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7172582
2140576094
2140576099
2140576115
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000015.10:g.67542218T>C , CM000677.2:g.67542218T>C
GRCh38
NC_000015.9:g.67834556T>C , CM000677.1:g.67834556T>C
GRCh37
NC_000015.8:g.65621610T>C
NCBI36
NG_029143.1:g.4536T>C
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