Canonical Allele Identifier: CA2702790368
Gene: CCR3 HGNC NCBI

Linked Data

dbSNP Id: rs2125922009
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46212336_46212339del , CM000665.2:g.46212336_46212339del GRCh38
NC_000003.11:g.46253827_46253830del , CM000665.1:g.46253827_46253830del GRCh37
NC_000003.10:g.46228831_46228834del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357422.2:c.-68+1429_-68+1432del ENSP00000350003.2:n.-68+1429_-68+1432del
XM_006712960.2:c.-68+1429_-68+1432del XP_006713023.1:n.-68+1429_-68+1432del
XM_011533334.1:c.-155+1429_-155+1432del XP_011531636.1:n.-155+1429_-155+1432del
XM_011533335.1:c.-149+1429_-149+1432del XP_011531637.1:n.-149+1429_-149+1432del
XM_006712960.3:c.-68+1429_-68+1432del XP_006713023.1:n.-68+1429_-68+1432del
XM_011533335.2:c.-149+1429_-149+1432del XP_011531637.1:n.-149+1429_-149+1432del
XM_017005686.1:c.-966+1429_-966+1432del XP_016861175.1:n.-966+1429_-966+1432del
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