ClinGen Allele Registry
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Canonical Allele Identifier:
CA14329762
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.78098377T>C
GRCh37
chr16:g.78132274T>C
Linked Data - Sequence & Population
gnomAD v2:
16:78132274 T / C
gnomAD v3:
16:78098377 T / C
gnomAD v4:
chr16-78098377-T-C
Joint Max Group AF
0.83498716 (EAS)
Genomes Max Group AF
0.83498716 (EAS)
Linked Data - NCBI & NCI
dbSNP:
10220974
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.78098377T>C , CM000678.2:g.78098377T>C
GRCh38
NC_000016.9:g.78132274T>C , CM000678.1:g.78132274T>C
GRCh37
NC_000016.8:g.76689775T>C
NCBI36
NG_011698.1:g.3724T>C
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