ClinGen Allele Registry
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Canonical Allele Identifier:
CA12560008
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.36788795G>A
GRCh37
chr7:g.36828400G>A
Linked Data - Sequence & Population
gnomAD v2:
7:36828400 G / A
gnomAD v3:
7:36788795 G / A
gnomAD v4:
chr7-36788795-G-A
Joint Max Group AF
0.19239393 (SAS)
Genomes Max Group AF
0.19239393 (SAS)
Linked Data - NCBI & NCI
dbSNP:
6963573
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.36788795G>A , CM000669.2:g.36788795G>A
GRCh38
NC_000007.13:g.36828400G>A , CM000669.1:g.36828400G>A
GRCh37
NC_000007.12:g.36794925G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'