ClinGen Allele Registry
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Canonical Allele Identifier:
CA14491392
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr17:g.34254422G>C
GRCh37
chr17:g.32581441G>C
Linked Data - Sequence & Population
gnomAD v2:
17:32581441 G / C
gnomAD v3:
17:34254422 G / C
gnomAD v4:
chr17-34254422-G-C
Joint Max Group AF
0.21441387 (NFE)
Genomes Max Group AF
0.21441387 (NFE)
Linked Data - NCBI & NCI
dbSNP:
3760396
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.34254422G>C , CM000679.2:g.34254422G>C
GRCh38
NC_000017.10:g.32581441G>C , CM000679.1:g.32581441G>C
GRCh37
NC_000017.9:g.29605554G>C
NCBI36
NG_012123.1:g.4146G>C
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