Canonical Allele Identifier: CA907585970
Gene: CCR3 HGNC NCBI

Linked Data

dbSNP Id: rs1373110734
gnomAD v3: 3-46240288-A-T
gnomAD v4: 3-46240288-A-T
MyVariant Identifiers: chr3:g.46281779A>T (hg19) chr3:g.46240288A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46240288A>T , CM000665.2:g.46240288A>T GRCh38
NC_000003.11:g.46281779A>T , CM000665.1:g.46281779A>T GRCh37
NC_000003.10:g.46256783A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000357422.2:c.-67-2114A>T ENSP00000350003.2:n.-67-2114A>T
XM_006712960.2:c.-67-2114A>T XP_006713023.1:n.-67-2114A>T
XM_011533334.1:c.-154-2114A>T XP_011531636.1:n.-154-2114A>T
XM_011533335.1:c.-148-2114A>T XP_011531637.1:n.-148-2114A>T
XM_006712960.3:c.-67-2114A>T XP_006713023.1:n.-67-2114A>T
XM_011533335.2:c.-148-2114A>T XP_011531637.1:n.-148-2114A>T
XM_017005686.1:c.-965-2114A>T XP_016861175.1:n.-965-2114A>T
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