Canonical Allele Identifier: CA1047506282

Gene: CCR3

Linked Data

• dbSNP Id: rs1700066250
• gnomAD v3: 3-46240278-A-T
• gnomAD v4: 3-46240278-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46240278A>T , CM000665.2:g.46240278A>T	GRCh38
NC_000003.11:g.46281769A>T , CM000665.1:g.46281769A>T	GRCh37
NC_000003.10:g.46256773A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000357422.2:c.-67-2124A>T	ENSP00000350003.2:n.-67-2124A>T
XM_006712960.2:c.-67-2124A>T	XP_006713023.1:n.-67-2124A>T
XM_011533334.1:c.-154-2124A>T	XP_011531636.1:n.-154-2124A>T
XM_011533335.1:c.-148-2124A>T	XP_011531637.1:n.-148-2124A>T
XM_006712960.3:c.-67-2124A>T	XP_006713023.1:n.-67-2124A>T
XM_011533335.2:c.-148-2124A>T	XP_011531637.1:n.-148-2124A>T
XM_017005686.1:c.-965-2124A>T	XP_016861175.1:n.-965-2124A>T