Canonical Allele Identifier: CA11568667
Gene: CCR3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46212298T>C , CM000665.2:g.46212298T>C GRCh38
NC_000003.11:g.46253789T>C , CM000665.1:g.46253789T>C GRCh37
NC_000003.10:g.46228793T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357422.2:c.-68+1391T>C ENSP00000350003.2:n.-68+1391T>C
XM_006712960.2:c.-68+1391T>C XP_006713023.1:n.-68+1391T>C
XM_011533334.1:c.-155+1391T>C XP_011531636.1:n.-155+1391T>C
XM_011533335.1:c.-149+1391T>C XP_011531637.1:n.-149+1391T>C
XM_006712960.3:c.-68+1391T>C XP_006713023.1:n.-68+1391T>C
XM_011533335.2:c.-149+1391T>C XP_011531637.1:n.-149+1391T>C
XM_017005686.1:c.-966+1391T>C XP_016861175.1:n.-966+1391T>C
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