ClinGen Allele Registry
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Canonical Allele Identifier:
CA14303928
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr16:g.82625589G>C
GRCh37
chr16:g.82659194G>C
Linked Data - Sequence & Population
gnomAD v2:
16:82659194 G / C
gnomAD v3:
16:82625589 G / C
gnomAD v4:
chr16-82625589-G-C
Joint Max Group AF
0.64954798 (NFE)
Genomes Max Group AF
0.64954798 (NFE)
Linked Data - NCBI & NCI
dbSNP:
7204454
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.82625589G>C , CM000678.2:g.82625589G>C
GRCh38
NC_000016.9:g.82659194G>C , CM000678.1:g.82659194G>C
GRCh37
NC_000016.8:g.81216695G>C
NCBI36
NG_052819.1:g.3796G>C
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