ClinGen Allele Registry
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Canonical Allele Identifier:
CA14979573
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr22:g.17084145G>A
GRCh37
chr22:g.17565035G>A
Linked Data - Sequence & Population
gnomAD v2:
22:17565035 G / A
gnomAD v3:
22:17084145 G / A
gnomAD v4:
chr22-17084145-G-A
Joint Max Group AF
0.95225246 (AFR)
Genomes Max Group AF
0.95225246 (AFR)
Linked Data - NCBI & NCI
dbSNP:
4819554
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.17084145G>A , CM000684.2:g.17084145G>A
GRCh38
NC_000022.10:g.17565035G>A , CM000684.1:g.17565035G>A
GRCh37
NC_000022.9:g.15945035G>A
NCBI36
NG_028257.1:g.4185G>A , LRG_355:g.4185G>A
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