Canonical Allele Identifier: CA2596730362

Gene: CCR3

Linked Data

• dbSNP Id: rs2125921988
• gnomAD v3: 3-46212218-T-A
• gnomAD v4: 3-46212218-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46212218T>A , CM000665.2:g.46212218T>A	GRCh38
NC_000003.11:g.46253709T>A , CM000665.1:g.46253709T>A	GRCh37
NC_000003.10:g.46228713T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357422.2:c.-68+1311T>A	ENSP00000350003.2:n.-68+1311T>A
XM_006712960.2:c.-68+1311T>A	XP_006713023.1:n.-68+1311T>A
XM_011533334.1:c.-155+1311T>A	XP_011531636.1:n.-155+1311T>A
XM_011533335.1:c.-149+1311T>A	XP_011531637.1:n.-149+1311T>A
XM_006712960.3:c.-68+1311T>A	XP_006713023.1:n.-68+1311T>A
XM_011533335.2:c.-149+1311T>A	XP_011531637.1:n.-149+1311T>A
XM_017005686.1:c.-966+1311T>A	XP_016861175.1:n.-966+1311T>A