ClinGen Allele Registry
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Canonical Allele Identifier:
CA15466354
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.32622945G>T
GRCh37
chr6:g.32590722G>T
Linked Data - Sequence & Population
gnomAD v2:
6:32590722 G / T
gnomAD v3:
6:32622945 G / T
gnomAD v4:
chr6-32622945-G-T
Joint Max Group AF
0.1560307 (NFE)
Genomes Max Group AF
0.1560307 (NFE)
Linked Data - NCBI & NCI
dbSNP:
17533090
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.32622945G>T , CM000668.2:g.32622945G>T
GRCh38
NC_000006.11:g.32590722G>T , CM000668.1:g.32590722G>T
GRCh37
NC_000006.10:g.32698700G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'