ClinGen Allele Registry
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Canonical Allele Identifier:
CA12438298
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr6:g.52185695C>T
GRCh37
chr6:g.52050493C>T
Linked Data - Sequence & Population
gnomAD v2:
6:52050493 C / T
gnomAD v3:
6:52185695 C / T
gnomAD v4:
chr6-52185695-C-T
Joint Max Group AF
0.75615355 (AMR)
Genomes Max Group AF
0.75615355 (AMR)
Linked Data - NCBI & NCI
dbSNP:
8193036
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.52185695C>T , CM000668.2:g.52185695C>T
GRCh38
NC_000006.11:g.52050493C>T , CM000668.1:g.52050493C>T
GRCh37
NC_000006.10:g.52158452C>T
NCBI36
NG_033021.1:g.4309C>T
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