Canonical Allele Identifier: CA1362021161
Gene: CCR3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46240266A= , CM000665.2:g.46240266A= GRCh38
NC_000003.11:g.46281757A= , CM000665.1:g.46281757A= GRCh37
NC_000003.10:g.46256761A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000357422.2:c.-67-2136A= ENSP00000350003.2:n.-67-2136A=
XM_006712960.2:c.-67-2136A= XP_006713023.1:n.-67-2136A=
XM_011533334.1:c.-154-2136A= XP_011531636.1:n.-154-2136A=
XM_011533335.1:c.-148-2136A= XP_011531637.1:n.-148-2136A=
XM_006712960.3:c.-67-2136A= XP_006713023.1:n.-67-2136A=
XM_011533335.2:c.-148-2136A= XP_011531637.1:n.-148-2136A=
XM_017005686.1:c.-965-2136A= XP_016861175.1:n.-965-2136A=