ClinGen Allele Registry
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Canonical Allele Identifier:
CA292868431
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.63474189G>A
GRCh37
chr17:g.61551550G>A
Linked Data - Sequence & Population
gnomAD v2:
17:61551550 G / A
gnomAD v3:
17:63474189 G / A
gnomAD v4:
chr17-63474189-G-A
Joint Max Group AF
0.17968245 (AFR)
Genomes Max Group AF
0.17968245 (AFR)
Linked Data - NCBI & NCI
dbSNP:
7213516
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.63474189G>A , CM000679.2:g.63474189G>A
GRCh38
NC_000017.10:g.61551550G>A , CM000679.1:g.61551550G>A
GRCh37
NC_000017.9:g.58905282G>A
NCBI36
NG_011648.1:g.2117G>A
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