ClinGen Allele Registry
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Canonical Allele Identifier:
CA14645314
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.47894860C>T
GRCh37
chr19:g.48398117C>T
Linked Data - Sequence & Population
gnomAD v2:
19:48398117 C / T
gnomAD v3:
19:47894860 C / T
gnomAD v4:
chr19-47894860-C-T
Joint Max Group AF
0.62648549 (AFR)
Genomes Max Group AF
0.62648549 (AFR)
Linked Data - NCBI & NCI
dbSNP:
2910397
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.47894860C>T , CM000681.2:g.47894860C>T
GRCh38
NC_000019.9:g.48398117C>T , CM000681.1:g.48398117C>T
GRCh37
NC_000019.8:g.53089929C>T
NCBI36
Search 100 bp 5'
Search 100 bp 3'