ClinGen Allele Registry
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Canonical Allele Identifier:
CA144362560
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.98489270T>G
GRCh37
chr6:g.98937146T>G
Linked Data - Sequence & Population
gnomAD v2:
6:98937146 T / G
gnomAD v3:
6:98489270 T / G
gnomAD v4:
chr6-98489270-T-G
Joint Max Group AF
0.37525248 (EAS)
Genomes Max Group AF
0.37525248 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2213553
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.98489270T>G , CM000668.2:g.98489270T>G
GRCh38
NC_000006.11:g.98937146T>G , CM000668.1:g.98937146T>G
GRCh37
NC_000006.10:g.99043867T>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'