Canonical Allele Identifier: CA1047506276
Gene: CCR3 HGNC NCBI

Linked Data

dbSNP Id: rs1700066098

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46240268_46240270del , CM000665.2:g.46240268_46240270del GRCh38
NC_000003.11:g.46281759_46281761del , CM000665.1:g.46281759_46281761del GRCh37
NC_000003.10:g.46256763_46256765del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000357422.2:c.-67-2134_-67-2132del ENSP00000350003.2:n.-67-2134_-67-2132del
XM_006712960.2:c.-67-2134_-67-2132del XP_006713023.1:n.-67-2134_-67-2132del
XM_011533334.1:c.-154-2134_-154-2132del XP_011531636.1:n.-154-2134_-154-2132del
XM_011533335.1:c.-148-2134_-148-2132del XP_011531637.1:n.-148-2134_-148-2132del
XM_006712960.3:c.-67-2134_-67-2132del XP_006713023.1:n.-67-2134_-67-2132del
XM_011533335.2:c.-148-2134_-148-2132del XP_011531637.1:n.-148-2134_-148-2132del
XM_017005686.1:c.-965-2134_-965-2132del XP_016861175.1:n.-965-2134_-965-2132del