ClinGen Allele Registry
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Canonical Allele Identifier:
CA12188054
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr6:g.32411712C>T
GRCh37
chr6:g.32379489C>T
Linked Data - Sequence & Population
gnomAD v2:
6:32379489 C / T
gnomAD v3:
6:32411712 C / T
gnomAD v4:
chr6-32411712-C-T
Joint Max Group AF
0.28744244 (AMR)
Genomes Max Group AF
0.28744244 (AMR)
Linked Data - NCBI & NCI
dbSNP:
9268516
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.32411712C>T , CM000668.2:g.32411712C>T
GRCh38
NC_000006.11:g.32379489C>T , CM000668.1:g.32379489C>T
GRCh37
NC_000006.10:g.32487467C>T
NCBI36
NG_054759.1:g.2168G>A
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