Canonical Allele Identifier: CA119356
Gene: CCR5 HGNC NCBI
CCR5AS HGNC NCBI

Linked Data

ClinVar Variation Id: 8186
ClinVar RCV Id: RCV000008668
dbSNP Id: rs1800452
ExAC: 3:46415061 G / A
gnomAD v2: 3-46415061-G-A
gnomAD v3: 3-46373570-G-A
gnomAD v4: 3-46373570-G-A
MyVariant Identifiers: chr3:g.46415061G>A (hg19) chr3:g.46373570G>A (hg38)
PubMed: PMID:9207783
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373570G>A , CM000665.2:g.46373570G>A GRCh38
NC_000003.11:g.46415061G>A , CM000665.1:g.46415061G>A GRCh37
NC_000003.10:g.46390065G>A NCBI36
NG_012637.1:g.8429G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.668G>A (CCR5) MANE Select ENSP00000292303.4:p.Arg223Gln
ENST00000292303.4:c.668G>A (CCR5) ENSP00000292303.4:p.Arg223Gln
ENST00000445772.1:c.668G>A (CCR5) ENSP00000404881.1:p.Arg223Gln
NM_000579.3:c.668G>A (CCR5) NP_000570.1:p.Arg223Gln
NM_001100168.1:c.668G>A (CCR5) NP_001093638.1:p.Arg223Gln
NR_125406.1:n.392-2153C>T (CCR5AS)
NM_000579.4:c.668G>A (CCR5) NP_000570.1:p.Arg223Gln
NM_001100168.2:c.668G>A (CCR5) NP_001093638.1:p.Arg223Gln
NM_001394783.1:c.668G>A (CCR5) MANE Select NP_001381712.1:p.Arg223Gln
Search 100 bp 5'
Search 100 bp 3'