Canonical Allele Identifier: CA1047506279
Gene: CCR3 HGNC NCBI

Linked Data

dbSNP Id: rs1700066215
gnomAD v3: 3-46240272-T-C
gnomAD v4: 3-46240272-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46240272T>C , CM000665.2:g.46240272T>C GRCh38
NC_000003.11:g.46281763T>C , CM000665.1:g.46281763T>C GRCh37
NC_000003.10:g.46256767T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000357422.2:c.-67-2130T>C ENSP00000350003.2:n.-67-2130T>C
XM_006712960.2:c.-67-2130T>C XP_006713023.1:n.-67-2130T>C
XM_011533334.1:c.-154-2130T>C XP_011531636.1:n.-154-2130T>C
XM_011533335.1:c.-148-2130T>C XP_011531637.1:n.-148-2130T>C
XM_006712960.3:c.-67-2130T>C XP_006713023.1:n.-67-2130T>C
XM_011533335.2:c.-148-2130T>C XP_011531637.1:n.-148-2130T>C
XM_017005686.1:c.-965-2130T>C XP_016861175.1:n.-965-2130T>C
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