ClinGen Allele Registry
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Canonical Allele Identifier:
CA14720568
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr19:g.21773334G>A
GRCh37
chr19:g.21956136G>A
Linked Data - Sequence & Population
gnomAD v2:
19:21956136 G / A
gnomAD v3:
19:21773334 G / A
gnomAD v4:
chr19-21773334-G-A
Joint Max Group AF
0.92566615 (EAS)
Genomes Max Group AF
0.92566615 (EAS)
Linked Data - NCBI & NCI
dbSNP:
8101143
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.21773334G>A , CM000681.2:g.21773334G>A
GRCh38
NC_000019.9:g.21956136G>A , CM000681.1:g.21956136G>A
GRCh37
NC_000019.8:g.21747976G>A
NCBI36
Search 100 bp 5'
Search 100 bp 3'