ClinGen Allele Registry
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Canonical Allele Identifier:
CA14949877
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.28765019C>T
GRCh37
chr22:g.29161007C>T
Linked Data - Sequence & Population
gnomAD v2:
22:29161007 C / T
gnomAD v3:
22:28765019 C / T
gnomAD v4:
chr22-28765019-C-T
Joint Max Group AF
0.38280695 (EAS)
Genomes Max Group AF
0.38280695 (EAS)
Linked Data - NCBI & NCI
dbSNP:
4820792
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.28765019C>T , CM000684.2:g.28765019C>T
GRCh38
NC_000022.10:g.29161007C>T , CM000684.1:g.29161007C>T
GRCh37
NC_000022.9:g.27491007C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'