ClinGen Allele Registry
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Canonical Allele Identifier:
CA12441458
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.32411959G>A
GRCh37
chr6:g.32379736G>A
Linked Data - Sequence & Population
gnomAD v2:
6:32379736 G / A
gnomAD v3:
6:32411959 G / A
gnomAD v4:
chr6-32411959-G-A
Joint Max Group AF
0.19961575 (EAS)
Genomes Max Group AF
0.19961575 (EAS)
Linked Data - NCBI & NCI
dbSNP:
9405098
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.32411959G>A , CM000668.2:g.32411959G>A
GRCh38
NC_000006.11:g.32379736G>A , CM000668.1:g.32379736G>A
GRCh37
NC_000006.10:g.32487714G>A
NCBI36
NG_054759.1:g.1921C>T
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