ClinGen Allele Registry
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Canonical Allele Identifier:
CA527766792
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.186681547G>T
GRCh37
chr1:g.186650679G>T
Linked Data - Sequence & Population
gnomAD v2:
1:186650679 G / T
Linked Data - NCBI & NCI
dbSNP:
1202496487
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.186681547G>T , CM000663.2:g.186681547G>T
GRCh38
NC_000001.10:g.186650679G>T , CM000663.1:g.186650679G>T
GRCh37
NC_000001.9:g.184917302G>T
NCBI36
NG_028206.2:g.3881C>A
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