Canonical Allele Identifier: CA73674706

Gene: CCR3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46264639G>T , CM000665.2:g.46264639G>T	GRCh38
NC_000003.11:g.46306130G>T , CM000665.1:g.46306130G>T	GRCh37
NC_000003.10:g.46281134G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395940.3:c.-11-509G>T MANE Select	ENSP00000379271.2:n.-11-509G>T
ENST00000357422.2:c.-11-509G>T	ENSP00000350003.2:n.-11-509G>T
ENST00000395940.2:c.-11-509G>T	ENSP00000379271.2:n.-11-509G>T
ENST00000452454.1:c.-12+184G>T	ENSP00000389336.1:n.-12+184G>T
ENST00000457243.1:c.-12+193G>T	ENSP00000401822.1:n.-12+193G>T
ENST00000475150.1:n.1066+184G>T
ENST00000484025.5:n.331G>T
ENST00000545097.1:c.52+184G>T	ENSP00000441600.1:n.52+184G>T
NM_001164680.1:c.43+193G>T	NP_001158152.1:n.43+193G>T
NM_001837.3:c.-11-509G>T	NP_001828.1:n.-11-509G>T
NM_178328.1:c.52+184G>T	NP_847898.1:n.52+184G>T
NM_178329.2:c.-11-509G>T	NP_847899.1:n.-11-509G>T
XM_006712960.2:c.-11-509G>T	XP_006713023.1:n.-11-509G>T
XM_011533334.1:c.52+184G>T	XP_011531636.1:n.52+184G>T
XM_011533335.1:c.-11-509G>T	XP_011531637.1:n.-11-509G>T
XM_006712960.3:c.-11-509G>T	XP_006713023.1:n.-11-509G>T
XM_011533335.2:c.-11-509G>T	XP_011531637.1:n.-11-509G>T
XM_017005685.1:c.154+184G>T	XP_016861174.1:n.154+184G>T
XM_017005686.1:c.154+184G>T	XP_016861175.1:n.154+184G>T
NM_178329.3:c.-11-509G>T MANE Select	NP_847899.1:n.-11-509G>T
NM_001164680.2:c.43+193G>T	NP_001158152.1:n.43+193G>T
NM_001837.4:c.-11-509G>T	NP_001828.1:n.-11-509G>T