ClinGen Allele Registry
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Canonical Allele Identifier:
CA14644114
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr19:g.44823511C>T
GRCh37
chr19:g.45326768C>T
Linked Data - Sequence & Population
gnomAD v2:
19:45326768 C / T
gnomAD v3:
19:44823511 C / T
gnomAD v4:
chr19-44823511-C-T
Joint Max Group AF
0.45882364 (SAS)
Genomes Max Group AF
0.45882364 (SAS)
Linked Data - NCBI & NCI
dbSNP:
1871045
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.44823511C>T , CM000681.2:g.44823511C>T
GRCh38
NC_000019.9:g.45326768C>T , CM000681.1:g.45326768C>T
GRCh37
NC_000019.8:g.50018608C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'