ClinGen Allele Registry
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Canonical Allele Identifier:
CA14767462
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr20:g.3081821G>T
GRCh37
chr20:g.3062467G>T
Linked Data - Sequence & Population
gnomAD v2:
20:3062467 G / T
gnomAD v3:
20:3081821 G / T
gnomAD v4:
chr20-3081821-G-T
Joint Max Group AF
0.44047979 (AMR)
Genomes Max Group AF
0.44047979 (AMR)
Linked Data - NCBI & NCI
dbSNP:
2740204
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.3081821G>T , CM000682.2:g.3081821G>T
GRCh38
NC_000020.10:g.3062467G>T , CM000682.1:g.3062467G>T
GRCh37
NC_000020.9:g.3010467G>T
NCBI36
NG_008663.1:g.7904C>A , LRG_715:g.7904C>A
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