ClinGen Allele Registry
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Canonical Allele Identifier:
CA283794626
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.74847922C>T
GRCh37
chr16:g.74881820C>T
Linked Data - Sequence & Population
gnomAD v2:
16:74881820 C / T
gnomAD v3:
16:74847922 C / T
gnomAD v4:
chr16-74847922-C-T
Joint Max Group AF
0.12121714 (AFR)
Genomes Max Group AF
0.12121714 (AFR)
Linked Data - NCBI & NCI
dbSNP:
16948255
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.74847922C>T , CM000678.2:g.74847922C>T
GRCh38
NC_000016.9:g.74881820C>T , CM000678.1:g.74881820C>T
GRCh37
NC_000016.8:g.73439321C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'