ClinGen Allele Registry
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Canonical Allele Identifier:
CA12423372
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.104921635A>G
GRCh37
chr6:g.105369510A>G
Linked Data - Sequence & Population
gnomAD v2:
6:105369510 A / G
gnomAD v3:
6:104921635 A / G
gnomAD v4:
chr6-104921635-A-G
Joint Max Group AF
0.67441422 (EAS)
Genomes Max Group AF
0.67441422 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4946651
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.104921635A>G , CM000668.2:g.104921635A>G
GRCh38
NC_000006.11:g.105369510A>G , CM000668.1:g.105369510A>G
GRCh37
NC_000006.10:g.105476203A>G
NCBI36
Search 100 bp 5'
Search 100 bp 3'