ClinGen Allele Registry
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Canonical Allele Identifier:
CA12212315
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.149441401A>G
GRCh37
chr6:g.149762537A>G
Linked Data - Sequence & Population
gnomAD v2:
6:149762537 A / G
gnomAD v3:
6:149441401 A / G
gnomAD v4:
chr6-149441401-A-G
Joint Max Group AF
0.73062528 (EAS)
Genomes Max Group AF
0.73062528 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2179367
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.149441401A>G , CM000668.2:g.149441401A>G
GRCh38
NC_000006.11:g.149762537A>G , CM000668.1:g.149762537A>G
GRCh37
NC_000006.10:g.149804230A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'