ClinGen Allele Registry
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Canonical Allele Identifier:
CA12133886
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr5:g.142544830T>C
GRCh37
chr5:g.141924395T>C
Linked Data - Sequence & Population
gnomAD v2:
5:141924395 T / C
gnomAD v3:
5:142544830 T / C
gnomAD v4:
chr5-142544830-T-C
Joint Max Group AF
0.62032213 (AFR)
Genomes Max Group AF
0.62032213 (AFR)
Linked Data - NCBI & NCI
dbSNP:
152439
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.142544830T>C , CM000667.2:g.142544830T>C
GRCh38
NC_000005.9:g.141924395T>C , CM000667.1:g.141924395T>C
GRCh37
NC_000005.8:g.141904579T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'