ClinGen Allele Registry
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Canonical Allele Identifier:
CA12638848
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr7:g.129077852G>A
GRCh37
chr7:g.128717906G>A
Linked Data - Sequence & Population
gnomAD v2:
7:128717906 G / A
gnomAD v3:
7:129077852 G / A
gnomAD v4:
chr7-129077852-G-A
Joint Max Group AF
0.15353671 (AMR)
Genomes Max Group AF
0.15353671 (AMR)
Linked Data - NCBI & NCI
dbSNP:
12537284
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.129077852G>A , CM000669.2:g.129077852G>A
GRCh38
NC_000007.13:g.128717906G>A , CM000669.1:g.128717906G>A
GRCh37
NC_000007.12:g.128505142G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'