ClinGen Allele Registry
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Canonical Allele Identifier:
CA783226119
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr19:g.1107036T>A
GRCh37
chr19:g.1107035T>A
Linked Data - Sequence & Population
gnomAD v3:
19:1107036 T / A
gnomAD v4:
chr19-1107036-T-A
Linked Data - NCBI & NCI
dbSNP:
2074451
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.1107036T>A , CM000681.2:g.1107036T>A
GRCh38
NC_000019.9:g.1107035T>A , CM000681.1:g.1107035T>A
GRCh37
NC_000019.8:g.1058035T>A
NCBI36
NG_050621.1:g.8111T>A
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