ClinGen Allele Registry
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Canonical Allele Identifier:
CA883288142
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.51462741C>G
GRCh37
chr19:g.51965995C>G
Linked Data - Sequence & Population
gnomAD v3:
19:51462741 C / G
gnomAD v4:
chr19-51462741-C-G
Linked Data - NCBI & NCI
dbSNP:
36498
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.51462741C>G , CM000681.2:g.51462741C>G
GRCh38
NC_000019.9:g.51965995C>G , CM000681.1:g.51965995C>G
GRCh37
NC_000019.8:g.56657807C>G
NCBI36
Search 100 bp 5'
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