Canonical Allele Identifier: CA352472850
Gene: CCR5 HGNC NCBI
CCR5AS HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.46415181T>A (hg19) chr3:g.46373690T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373690T>A , CM000665.2:g.46373690T>A GRCh38
NC_000003.11:g.46415181T>A , CM000665.1:g.46415181T>A GRCh37
NC_000003.10:g.46390185T>A NCBI36
NG_012637.1:g.8549T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000292303.5:c.788T>A (CCR5) MANE Select ENSP00000292303.4:p.Phe263Tyr
ENST00000292303.4:c.788T>A (CCR5) ENSP00000292303.4:p.Phe263Tyr
ENST00000445772.1:c.788T>A (CCR5) ENSP00000404881.1:p.Phe263Tyr
NM_000579.3:c.788T>A (CCR5) NP_000570.1:p.Phe263Tyr
NM_001100168.1:c.788T>A (CCR5) NP_001093638.1:p.Phe263Tyr
NR_125406.1:n.392-2273A>T (CCR5AS)
NM_000579.4:c.788T>A (CCR5) NP_000570.1:p.Phe263Tyr
NM_001100168.2:c.788T>A (CCR5) NP_001093638.1:p.Phe263Tyr
NM_001394783.1:c.788T>A (CCR5) MANE Select NP_001381712.1:p.Phe263Tyr
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