ClinGen Allele Registry
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Canonical Allele Identifier:
CA12755593
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr8:g.19968862G>A
GRCh37
chr8:g.19826373G>A
Linked Data - Sequence & Population
gnomAD v2:
8:19826373 G / A
gnomAD v3:
8:19968862 G / A
gnomAD v4:
chr8-19968862-G-A
Joint Max Group AF
0.77956727 (AFR)
Genomes Max Group AF
0.77956727 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2197089
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000008.11:g.19968862G>A , CM000670.2:g.19968862G>A
GRCh38
NC_000008.10:g.19826373G>A , CM000670.1:g.19826373G>A
GRCh37
NC_000008.9:g.19870653G>A
NCBI36
NG_008855.1:g.34792G>A
NG_008855.2:g.72146G>A
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