ClinGen Allele Registry
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Canonical Allele Identifier:
CA15913058
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.76503318G>A
GRCh37
chr17:g.74499400G>A
Linked Data - Sequence & Population
gnomAD v2:
17:74499400 G / A
gnomAD v3:
17:76503318 G / A
gnomAD v4:
chr17-76503318-G-A
Joint Max Group AF
0.39116236 (SAS)
Genomes Max Group AF
0.39116236 (SAS)
Linked Data - NCBI & NCI
dbSNP:
12948783
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.76503318G>A , CM000679.2:g.76503318G>A
GRCh38
NC_000017.10:g.74499400G>A , CM000679.1:g.74499400G>A
GRCh37
NC_000017.9:g.72010995G>A
NCBI36
NG_032852.1:g.3110C>T , LRG_532:g.3110C>T
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