ClinGen Allele Registry
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Canonical Allele Identifier:
CA783226145
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.1107065T>G
GRCh37
chr19:g.1107064T>G
Linked Data - Sequence & Population
gnomAD v3:
19:1107065 T / G
gnomAD v4:
chr19-1107065-T-G
Linked Data - NCBI & NCI
dbSNP:
1370247606
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.1107065T>G , CM000681.2:g.1107065T>G
GRCh38
NC_000019.9:g.1107064T>G , CM000681.1:g.1107064T>G
GRCh37
NC_000019.8:g.1058064T>G
NCBI36
NG_050621.1:g.8140T>G
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