ClinGen Allele Registry
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Canonical Allele Identifier:
CA12186444
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr6:g.29952759G>T
GRCh37
chr6:g.29920536G>T
Linked Data - Sequence & Population
gnomAD v2:
6:29920536 G / T
gnomAD v3:
6:29952759 G / T
gnomAD v4:
chr6-29952759-G-T
Joint Max Group AF
0.73752808 (AMR)
Genomes Max Group AF
0.73752808 (AMR)
Linked Data - NCBI & NCI
dbSNP:
2975042
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.29952759G>T , CM000668.2:g.29952759G>T
GRCh38
NC_000006.11:g.29920536G>T , CM000668.1:g.29920536G>T
GRCh37
NC_000006.10:g.30028515G>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'