ClinGen Allele Registry
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Canonical Allele Identifier:
CA14733526
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.5841345G>T
GRCh37
chr19:g.5841356G>T
Linked Data - Sequence & Population
gnomAD v2:
19:5841356 G / T
gnomAD v3:
19:5841345 G / T
gnomAD v4:
chr19-5841345-G-T
Joint Max Group AF
0.30222777 (EAS)
Genomes Max Group AF
0.30222777 (EAS)
Linked Data - NCBI & NCI
dbSNP:
3760775
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.5841345G>T , CM000681.2:g.5841345G>T
GRCh38
NC_000019.9:g.5841356G>T , CM000681.1:g.5841356G>T
GRCh37
NC_000019.8:g.5792356G>T
NCBI36
NG_007482.1:g.15130C>A
NG_007505.1:g.3387C>A
NG_007482.2:g.20778C>A
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