ClinGen Allele Registry
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Canonical Allele Identifier:
CA14387197
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr17:g.74769592G>A
GRCh37
chr17:g.72765731G>A
Linked Data - Sequence & Population
gnomAD v2:
17:72765731 G / A
gnomAD v3:
17:74769592 G / A
gnomAD v4:
chr17-74769592-G-A
Joint Max Group AF
0.44354424 (NFE)
Genomes Max Group AF
0.44354424 (NFE)
Linked Data - NCBI & NCI
dbSNP:
734232
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.74769592G>A , CM000679.2:g.74769592G>A
GRCh38
NC_000017.10:g.72765731G>A , CM000679.1:g.72765731G>A
GRCh37
NC_000017.9:g.70277326G>A
NCBI36
NG_013022.1:g.25969G>A
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