ClinGen Allele Registry
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Canonical Allele Identifier:
CA14289491
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.85976134T>C
GRCh37
chr16:g.86009740T>C
Linked Data - Sequence & Population
gnomAD v2:
16:86009740 T / C
gnomAD v3:
16:85976134 T / C
gnomAD v4:
chr16-85976134-T-C
Joint Max Group AF
0.26857508 (SAS)
Genomes Max Group AF
0.26857508 (SAS)
Linked Data - NCBI & NCI
dbSNP:
16940186
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.85976134T>C , CM000678.2:g.85976134T>C
GRCh38
NC_000016.9:g.86009740T>C , CM000678.1:g.86009740T>C
GRCh37
NC_000016.8:g.84567241T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'