ClinGen Allele Registry
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Canonical Allele Identifier:
CA12840075
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.73361956C>T
GRCh37
chr8:g.74274191C>T
Linked Data - Sequence & Population
gnomAD v2:
8:74274191 C / T
gnomAD v3:
8:73361956 C / T
gnomAD v4:
chr8-73361956-C-T
Joint Max Group AF
0.50299598 (EAS)
Genomes Max Group AF
0.50299598 (EAS)
Linked Data - NCBI & NCI
dbSNP:
12679254
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.73361956C>T , CM000670.2:g.73361956C>T
GRCh38
NC_000008.10:g.74274191C>T , CM000670.1:g.74274191C>T
GRCh37
NC_000008.9:g.74436745C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'