Canonical Allele Identifier: CA1362021177
Gene: CCR3 HGNC NCBI

Linked Data

dbSNP Id: rs1700066504
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46240296G>A , CM000665.2:g.46240296G>A GRCh38
NC_000003.11:g.46281787G>A , CM000665.1:g.46281787G>A GRCh37
NC_000003.10:g.46256791G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000357422.2:c.-67-2106G>A ENSP00000350003.2:n.-67-2106G>A
XM_006712960.2:c.-67-2106G>A XP_006713023.1:n.-67-2106G>A
XM_011533334.1:c.-154-2106G>A XP_011531636.1:n.-154-2106G>A
XM_011533335.1:c.-148-2106G>A XP_011531637.1:n.-148-2106G>A
XM_006712960.3:c.-67-2106G>A XP_006713023.1:n.-67-2106G>A
XM_011533335.2:c.-148-2106G>A XP_011531637.1:n.-148-2106G>A
XM_017005686.1:c.-965-2106G>A XP_016861175.1:n.-965-2106G>A
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