ClinGen Allele Registry
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Canonical Allele Identifier:
CA12344791
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.33089934G>A
GRCh37
chr6:g.33057711G>A
Linked Data - Sequence & Population
gnomAD v2:
6:33057711 G / A
gnomAD v3:
6:33089934 G / A
gnomAD v4:
chr6-33089934-G-A
Joint Max Group AF
0.62240973 (EAS)
Genomes Max Group AF
0.62240973 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3117225
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.33089934G>A , CM000668.2:g.33089934G>A
GRCh38
NC_000006.11:g.33057711G>A , CM000668.1:g.33057711G>A
GRCh37
NC_000006.10:g.33165689G>A
NCBI36
NG_033242.1:g.19009G>A
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