ClinGen Allele Registry
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Canonical Allele Identifier:
CA265627060
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr14:g.91960878A>C
GRCh37
chr14:g.92427222A>C
Linked Data - Sequence & Population
gnomAD v2:
14:92427222 A / C
gnomAD v3:
14:91960878 A / C
gnomAD v4:
chr14-91960878-A-C
Joint Max Group AF
0.53879955 (AFR)
Genomes Max Group AF
0.53879955 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7153027
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000014.9:g.91960878A>C , CM000676.2:g.91960878A>C
GRCh38
NC_000014.8:g.92427222A>C , CM000676.1:g.92427222A>C
GRCh37
NC_000014.7:g.91496975A>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'