ClinGen Allele Registry
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Canonical Allele Identifier:
CA14694622
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.1039411C>G
GRCh37
chr19:g.1039410C>G
Linked Data - Sequence & Population
gnomAD v2:
19:1039410 C / G
gnomAD v3:
19:1039411 C / G
gnomAD v4:
chr19-1039411-C-G
Joint Max Group AF
0.1923774 (NFE)
Genomes Max Group AF
0.1923774 (NFE)
Linked Data - NCBI & NCI
dbSNP:
3795064
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.1039411C>G , CM000681.2:g.1039411C>G
GRCh38
NC_000019.9:g.1039410C>G , CM000681.1:g.1039410C>G
GRCh37
NC_000019.8:g.990410C>G
NCBI36
NG_046909.1:g.4309C>G
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