ClinGen Allele Registry
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Canonical Allele Identifier:
CA14306778
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr16:g.56957451C>T
GRCh37
chr16:g.56991363C>T
Linked Data - Sequence & Population
gnomAD v2:
16:56991363 C / T
gnomAD v3:
16:56957451 C / T
gnomAD v4:
chr16-56957451-C-T
Joint Max Group AF
0.32226913 (SAS)
Genomes Max Group AF
0.32226913 (SAS)
Linked Data - NCBI & NCI
dbSNP:
183130
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.56957451C>T , CM000678.2:g.56957451C>T
GRCh38
NC_000016.9:g.56991363C>T , CM000678.1:g.56991363C>T
GRCh37
NC_000016.8:g.55548864C>T
NCBI36
NG_008952.1:g.529C>T
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