Canonical Allele Identifier: CA1047510382
Gene: CCR3 HGNC NCBI

Linked Data

dbSNP Id: rs1699722340
gnomAD v3: 3-46212202-C-T
gnomAD v4: 3-46212202-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46212202C>T , CM000665.2:g.46212202C>T GRCh38
NC_000003.11:g.46253693C>T , CM000665.1:g.46253693C>T GRCh37
NC_000003.10:g.46228697C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000357422.2:c.-68+1295C>T ENSP00000350003.2:n.-68+1295C>T
XM_006712960.2:c.-68+1295C>T XP_006713023.1:n.-68+1295C>T
XM_011533334.1:c.-155+1295C>T XP_011531636.1:n.-155+1295C>T
XM_011533335.1:c.-149+1295C>T XP_011531637.1:n.-149+1295C>T
XM_006712960.3:c.-68+1295C>T XP_006713023.1:n.-68+1295C>T
XM_011533335.2:c.-149+1295C>T XP_011531637.1:n.-149+1295C>T
XM_017005686.1:c.-966+1295C>T XP_016861175.1:n.-966+1295C>T