Canonical Allele Identifier: CA907572345

Gene: CCR3

Linked Data

• dbSNP Id: rs1265798767
• MyVariant Identifiers: chr3:g.46253695_46253700del (hg19) ; chr3:g.46212204_46212209del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46212205_46212210del , CM000665.2:g.46212205_46212210del	GRCh38
NC_000003.11:g.46253696_46253701del , CM000665.1:g.46253696_46253701del	GRCh37
NC_000003.10:g.46228700_46228705del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357422.2:c.-68+1298_-68+1303del	ENSP00000350003.2:n.-68+1298_-68+1303del
XM_006712960.2:c.-68+1298_-68+1303del	XP_006713023.1:n.-68+1298_-68+1303del
XM_011533334.1:c.-155+1298_-155+1303del	XP_011531636.1:n.-155+1298_-155+1303del
XM_011533335.1:c.-149+1298_-149+1303del	XP_011531637.1:n.-149+1298_-149+1303del
XM_006712960.3:c.-68+1298_-68+1303del	XP_006713023.1:n.-68+1298_-68+1303del
XM_011533335.2:c.-149+1298_-149+1303del	XP_011531637.1:n.-149+1298_-149+1303del
XM_017005686.1:c.-966+1298_-966+1303del	XP_016861175.1:n.-966+1298_-966+1303del