ClinGen Allele Registry
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Canonical Allele Identifier:
CA305878671
Gene: CLEC4OP
HGNC
NCBI
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chr19:g.15848390G>A
GRCh37
chr19:g.15959200G>A
Linked Data - Sequence & Population
gnomAD v2:
19:15959200 G / A
gnomAD v3:
19:15848390 G / A
gnomAD v4:
chr19-15848390-G-A
Joint Max Group AF
0.41831258 (MID)
Genomes Max Group AF
0.41103484 (SAS)
Linked Data - NCBI & NCI
dbSNP:
2189784
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.15848390G>A , CM000681.2:g.15848390G>A
GRCh38
NC_000019.9:g.15959200G>A , CM000681.1:g.15959200G>A
GRCh37
NC_000019.8:g.15820200G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000692445.1:n.202-2027C>T
Search 100 bp 5'
Search 100 bp 3'