Canonical Allele Identifier: CA11581628
Gene: CCR3 HGNC NCBI

Linked Data

dbSNP Id: rs17282391
gnomAD v2: 3-46179481-A-G
gnomAD v3: 3-46137989-A-G
gnomAD v4: 3-46137989-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46137989A>G , CM000665.2:g.46137989A>G GRCh38
NC_000003.11:g.46179481A>G , CM000665.1:g.46179481A>G GRCh37
NC_000003.10:g.46154485A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000684109.1:n.691+6409A>G
XR_940804.1:n.687+6409A>G
XR_940806.1:n.201+6895A>G
XR_940804.2:n.691+6409A>G