ClinGen Allele Registry
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Canonical Allele Identifier:
CA14329392
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.76844965G>A
GRCh37
chr16:g.76878862G>A
Linked Data - Sequence & Population
gnomAD v2:
16:76878862 G / A
gnomAD v3:
16:76844965 G / A
gnomAD v4:
chr16-76844965-G-A
Joint Max Group AF
0.37071737 (AFR)
Genomes Max Group AF
0.37071737 (AFR)
Linked Data - NCBI & NCI
dbSNP:
13330107
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.76844965G>A , CM000678.2:g.76844965G>A
GRCh38
NC_000016.9:g.76878862G>A , CM000678.1:g.76878862G>A
GRCh37
NC_000016.8:g.75436363G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'