ClinGen Allele Registry
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Canonical Allele Identifier:
CA13213496
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr10:g.6066476G>A
GRCh37
chr10:g.6108439G>A
Linked Data - Sequence & Population
gnomAD v2:
10:6108439 G / A
gnomAD v3:
10:6066476 G / A
gnomAD v4:
chr10-6066476-G-A
Joint Max Group AF
0.36445619 (AMR)
Genomes Max Group AF
0.36445619 (AMR)
Linked Data - NCBI & NCI
dbSNP:
4147359
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.6066476G>A , CM000672.2:g.6066476G>A
GRCh38
NC_000010.10:g.6108439G>A , CM000672.1:g.6108439G>A
GRCh37
NC_000010.9:g.6148445G>A
NCBI36
NG_007403.1:g.834C>T , LRG_73:g.834C>T
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