ClinGen Allele Registry
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Canonical Allele Identifier:
CA572783966
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.12020180T>C
GRCh37
chr7:g.12059806T>C
Linked Data - Sequence & Population
gnomAD v2:
7:12059806 T / C
gnomAD v3:
7:12020180 T / C
gnomAD v4:
chr7-12020180-T-C
Linked Data - NCBI & NCI
dbSNP:
769111
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.12020180T>C , CM000669.2:g.12020180T>C
GRCh38
NC_000007.13:g.12059806T>C , CM000669.1:g.12059806T>C
GRCh37
NC_000007.12:g.12026331T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'