Canonical Allele Identifier: CA11442301

Gene: CCR3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46213300T>C , CM000665.2:g.46213300T>C	GRCh38
NC_000003.11:g.46254791T>C , CM000665.1:g.46254791T>C	GRCh37
NC_000003.10:g.46229795T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357422.2:c.-68+2393T>C	ENSP00000350003.2:n.-68+2393T>C
XM_006712960.2:c.-68+2393T>C	XP_006713023.1:n.-68+2393T>C
XM_011533334.1:c.-155+2393T>C	XP_011531636.1:n.-155+2393T>C
XM_011533335.1:c.-149+2393T>C	XP_011531637.1:n.-149+2393T>C
XM_006712960.3:c.-68+2393T>C	XP_006713023.1:n.-68+2393T>C
XM_011533335.2:c.-149+2393T>C	XP_011531637.1:n.-149+2393T>C
XM_017005686.1:c.-966+2393T>C	XP_016861175.1:n.-966+2393T>C