ClinGen Allele Registry
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Canonical Allele Identifier:
CA728696049
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr1:g.186681658G>A
GRCh37
chr1:g.186650790G>A
Linked Data - NCBI & NCI
dbSNP:
1299894977
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.186681658G>A , CM000663.2:g.186681658G>A
GRCh38
NC_000001.10:g.186650790G>A , CM000663.1:g.186650790G>A
GRCh37
NC_000001.9:g.184917413G>A
NCBI36
NG_028206.2:g.3770C>T
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