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Canonical Allele Identifier:
CA783689228
Gene: CLEC4OP
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr19:g.15848390G>T
GRCh37
chr19:g.15959200G>T
Linked Data - NCBI & NCI
dbSNP:
2189784
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000019.10:g.15848390G>T , CM000681.2:g.15848390G>T
GRCh38
NC_000019.9:g.15959200G>T , CM000681.1:g.15959200G>T
GRCh37
NC_000019.8:g.15820200G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000692445.1:n.202-2027C>A
Search 100 bp 5'
Search 100 bp 3'