ClinGen Allele Registry
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Canonical Allele Identifier:
CA13844172
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr13:g.45326132G>A
GRCh37
chr13:g.45900267G>A
Linked Data - Sequence & Population
gnomAD v2:
13:45900267 G / A
gnomAD v3:
13:45326132 G / A
gnomAD v4:
chr13-45326132-G-A
Joint Max Group AF
0.11496034 (AFR)
Genomes Max Group AF
0.11496034 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7323755
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000013.11:g.45326132G>A , CM000675.2:g.45326132G>A
GRCh38
NC_000013.10:g.45900267G>A , CM000675.1:g.45900267G>A
GRCh37
NC_000013.9:g.44798267G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'