Canonical Allele Identifier: CA1362021204
Gene: CCR3 HGNC NCBI

Linked Data

dbSNP Id: rs1700067600

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46240380A>G , CM000665.2:g.46240380A>G GRCh38
NC_000003.11:g.46281871A>G , CM000665.1:g.46281871A>G GRCh37
NC_000003.10:g.46256875A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357422.2:c.-67-2022A>G ENSP00000350003.2:n.-67-2022A>G
XM_006712960.2:c.-67-2022A>G XP_006713023.1:n.-67-2022A>G
XM_011533334.1:c.-154-2022A>G XP_011531636.1:n.-154-2022A>G
XM_011533335.1:c.-148-2022A>G XP_011531637.1:n.-148-2022A>G
XM_006712960.3:c.-67-2022A>G XP_006713023.1:n.-67-2022A>G
XM_011533335.2:c.-148-2022A>G XP_011531637.1:n.-148-2022A>G
XM_017005686.1:c.-965-2022A>G XP_016861175.1:n.-965-2022A>G