Canonical Allele Identifier: CA1362009195
Gene: CCR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46212213_46212214delinsAC , CM000665.2:g.46212213_46212214delinsAC GRCh38
NC_000003.11:g.46253704_46253705delinsAC , CM000665.1:g.46253704_46253705delinsAC GRCh37
NC_000003.10:g.46228708_46228709delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357422.2:c.-68+1306_-68+1307delinsAC ENSP00000350003.2:n.-68+1306_-68+1307delinsAC
XM_006712960.2:c.-68+1306_-68+1307delinsAC XP_006713023.1:n.-68+1306_-68+1307delinsAC
XM_011533334.1:c.-155+1306_-155+1307delinsAC XP_011531636.1:n.-155+1306_-155+1307delinsAC
XM_011533335.1:c.-149+1306_-149+1307delinsAC XP_011531637.1:n.-149+1306_-149+1307delinsAC
XM_006712960.3:c.-68+1306_-68+1307delinsAC XP_006713023.1:n.-68+1306_-68+1307delinsAC
XM_011533335.2:c.-149+1306_-149+1307delinsAC XP_011531637.1:n.-149+1306_-149+1307delinsAC
XM_017005686.1:c.-966+1306_-966+1307delinsAC XP_016861175.1:n.-966+1306_-966+1307delinsAC