ClinGen Allele Registry
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Canonical Allele Identifier:
CA16448557
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr12:g.71938143G>T
GRCh37
chr12:g.72331923G>T
Linked Data - Sequence & Population
gnomAD v2:
12:72331923 G / T
gnomAD v3:
12:71938143 G / T
gnomAD v4:
chr12-71938143-G-T
Joint Max Group AF
0.52583932 (EAS)
Genomes Max Group AF
0.52583932 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4570625
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.71938143G>T , CM000674.2:g.71938143G>T
GRCh38
NC_000012.11:g.72331923G>T , CM000674.1:g.72331923G>T
GRCh37
NC_000012.10:g.70618190G>T
NCBI36
NG_008279.1:g.4298G>T
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