Canonical Allele Identifier: CA73798410
Gene: CCR3 HGNC NCBI

Linked Data

dbSNP Id: rs887920465
gnomAD v2: 3-46253836-G-A
gnomAD v3: 3-46212345-G-A
gnomAD v4: 3-46212345-G-A
MyVariant Identifiers: chr3:g.46253836G>A (hg19) chr3:g.46212345G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46212345G>A , CM000665.2:g.46212345G>A GRCh38
NC_000003.11:g.46253836G>A , CM000665.1:g.46253836G>A GRCh37
NC_000003.10:g.46228840G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357422.2:c.-68+1438G>A ENSP00000350003.2:n.-68+1438G>A
XM_006712960.2:c.-68+1438G>A XP_006713023.1:n.-68+1438G>A
XM_011533334.1:c.-155+1438G>A XP_011531636.1:n.-155+1438G>A
XM_011533335.1:c.-149+1438G>A XP_011531637.1:n.-149+1438G>A
XM_006712960.3:c.-68+1438G>A XP_006713023.1:n.-68+1438G>A
XM_011533335.2:c.-149+1438G>A XP_011531637.1:n.-149+1438G>A
XM_017005686.1:c.-966+1438G>A XP_016861175.1:n.-966+1438G>A
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