ClinGen Allele Registry
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Canonical Allele Identifier:
CA303995940
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.1106945G>T
GRCh37
chr19:g.1106944G>T
Linked Data - Sequence & Population
gnomAD v3:
19:1106945 G / T
gnomAD v4:
chr19-1106945-G-T
Joint Max Group AF
0.00004737 (AFR)
Genomes Max Group AF
0.00004737 (AFR)
Linked Data - NCBI & NCI
dbSNP:
925084415
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.1106945G>T , CM000681.2:g.1106945G>T
GRCh38
NC_000019.9:g.1106944G>T , CM000681.1:g.1106944G>T
GRCh37
NC_000019.8:g.1057944G>T
NCBI36
NG_050621.1:g.8020G>T
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