ClinGen Allele Registry
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Canonical Allele Identifier:
CA12223756
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.7719826G>A
GRCh37
chr6:g.7720059G>A
Linked Data - Sequence & Population
gnomAD v2:
6:7720059 G / A
gnomAD v3:
6:7719826 G / A
gnomAD v4:
chr6-7719826-G-A
Joint Max Group AF
0.51477952 (SAS)
Genomes Max Group AF
0.51477952 (SAS)
Linked Data - NCBI & NCI
dbSNP:
12198986
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.7719826G>A , CM000668.2:g.7719826G>A
GRCh38
NC_000006.11:g.7720059G>A , CM000668.1:g.7720059G>A
GRCh37
NC_000006.10:g.7665058G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'