Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.46373082G= , CM000665.2:g.46373082G= | GRCh38 |
| NC_000003.11:g.46414573G= , CM000665.1:g.46414573G= | GRCh37 |
| NC_000003.10:g.46389577G= | NCBI36 |
| NG_012637.1:g.7941G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001394783.1:c.180G= (CCR5) MANE Select | NP_001381712.1:p.Arg60= |
| ENST00000292303.5:c.180G= (CCR5) MANE Select | ENSP00000292303.4:p.Arg60= |
| NM_000579.3:c.180G= (CCR5) | NP_000570.1:p.Arg60= |
| NM_000579.4:c.180G= (CCR5) | NP_000570.1:p.Arg60= |
| NM_001100168.1:c.180G= (CCR5) | NP_001093638.1:p.Arg60= |
| NM_001100168.2:c.180G= (CCR5) | NP_001093638.1:p.Arg60= |
| NR_125406.1:n.392-1665C= (CCR5AS) | |
| ENST00000292303.4:c.180G= (CCR5) | ENSP00000292303.4:p.Arg60= |
| ENST00000445772.1:c.180G= (CCR5) | ENSP00000404881.1:p.Arg60= |