ClinGen Allele Registry
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Canonical Allele Identifier:
CA120239692
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr5:g.63962787C>T
GRCh37
chr5:g.63258614C>T
Linked Data - Sequence & Population
gnomAD v2:
5:63258614 C / T
gnomAD v3:
5:63962787 C / T
gnomAD v4:
chr5-63962787-C-T
Joint Max Group AF
0.03017423 (EAS)
Genomes Max Group AF
0.03017423 (EAS)
Linked Data - NCBI & NCI
dbSNP:
113195492
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.63962787C>T , CM000667.2:g.63962787C>T
GRCh38
NC_000005.9:g.63258614C>T , CM000667.1:g.63258614C>T
GRCh37
NC_000005.8:g.63294370C>T
NCBI36
NG_032816.1:g.4506G>A
Search 100 bp 5'
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