ClinGen Allele Registry
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Canonical Allele Identifier:
CA14639909
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.29580124C>G
GRCh37
chr19:g.30071031C>G
Linked Data - Sequence & Population
gnomAD v2:
19:30071031 C / G
gnomAD v3:
19:29580124 C / G
gnomAD v4:
chr19-29580124-C-G
Joint Max Group AF
0.71422099 (AMR)
Genomes Max Group AF
0.71422099 (AMR)
Linked Data - NCBI & NCI
dbSNP:
11670734
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.29580124C>G , CM000681.2:g.29580124C>G
GRCh38
NC_000019.9:g.30071031C>G , CM000681.1:g.30071031C>G
GRCh37
NC_000019.8:g.34762871C>G
NCBI36
Search 100 bp 5'
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