ClinGen Allele Registry
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Canonical Allele Identifier:
CA632881511
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.38645889T>A
GRCh37
chr19:g.39136529T>A
Linked Data - Sequence & Population
gnomAD v2:
19:39136529 T / A
gnomAD v3:
19:38645889 T / A
gnomAD v4:
chr19-38645889-T-A
Linked Data - NCBI & NCI
dbSNP:
1445586090
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.38645889T>A , CM000681.2:g.38645889T>A
GRCh38
NC_000019.9:g.39136529T>A , CM000681.1:g.39136529T>A
GRCh37
NC_000019.8:g.43828369T>A
NCBI36
NG_007082.2:g.3203T>A
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