Canonical Allele Identifier: CA2354665
Gene: CCR5 HGNC NCBI
CCR5AS HGNC NCBI

Linked Data

dbSNP Id: rs376687230
ExAC: 3:46414899 C / A
gnomAD v2: 3-46414899-C-A
gnomAD v3: 3-46373408-C-A
gnomAD v4: 3-46373408-C-A
MyVariant Identifiers: chr3:g.46414899C>A (hg19) chr3:g.46373408C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373408C>A , CM000665.2:g.46373408C>A GRCh38
NC_000003.11:g.46414899C>A , CM000665.1:g.46414899C>A GRCh37
NC_000003.10:g.46389903C>A NCBI36
NG_012637.1:g.8267C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.506C>A (CCR5) MANE Select ENSP00000292303.4:p.Ser169Tyr
ENST00000292303.4:c.506C>A (CCR5) ENSP00000292303.4:p.Ser169Tyr
ENST00000445772.1:c.506C>A (CCR5) ENSP00000404881.1:p.Ser169Tyr
NM_000579.3:c.506C>A (CCR5) NP_000570.1:p.Ser169Tyr
NM_001100168.1:c.506C>A (CCR5) NP_001093638.1:p.Ser169Tyr
NR_125406.1:n.392-1991G>T (CCR5AS)
NM_000579.4:c.506C>A (CCR5) NP_000570.1:p.Ser169Tyr
NM_001100168.2:c.506C>A (CCR5) NP_001093638.1:p.Ser169Tyr
NM_001394783.1:c.506C>A (CCR5) MANE Select NP_001381712.1:p.Ser169Tyr
Search 100 bp 5'
Search 100 bp 3'