Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10279982C= , CM000681.2:g.10279982C= | GRCh38 |
| NC_000019.9:g.10390658C= , CM000681.1:g.10390658C= | GRCh37 |
| NC_000019.8:g.10251658C= | NCBI36 |
| NG_012083.1:g.14142C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000201.3:c.332-3499C= (ICAM1) MANE Select | NP_000192.2:n.332-3499C= |
| ENST00000264832.8:c.332-3499C= (ICAM1) MANE Select | ENSP00000264832.2:n.332-3499C= |
| NM_000201.2:c.332-3499C= (ICAM1) | NP_000192.2:n.332-3499C= |
| ENST00000264832.7:c.332-3499C= (ICAM1) | ENSP00000264832.2:n.332-3499C= |
| ENST00000423829.2:c.68-4147C= (ICAM1) | ENSP00000413124.2:n.68-4147C= |
| ENST00000588645.1:c.332-3499C= (ICAM1) | ENSP00000465680.1:n.332-3499C= |
| XR_936313.1:n.154+3339G= (LIMASI) | |
| XR_936314.1:n.154+3339G= (LIMASI) |