Canonical Allele Identifier: CA1362021153
Gene: CCR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46240253C= , CM000665.2:g.46240253C= GRCh38
NC_000003.11:g.46281744C= , CM000665.1:g.46281744C= GRCh37
NC_000003.10:g.46256748C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000357422.2:c.-67-2149C= ENSP00000350003.2:n.-67-2149C=
XM_006712960.2:c.-67-2149C= XP_006713023.1:n.-67-2149C=
XM_011533334.1:c.-154-2149C= XP_011531636.1:n.-154-2149C=
XM_011533335.1:c.-148-2149C= XP_011531637.1:n.-148-2149C=
XM_006712960.3:c.-67-2149C= XP_006713023.1:n.-67-2149C=
XM_011533335.2:c.-148-2149C= XP_011531637.1:n.-148-2149C=
XM_017005686.1:c.-965-2149C= XP_016861175.1:n.-965-2149C=