Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10272527C>T , CM000681.2:g.10272527C>T | GRCh38 |
| NC_000019.9:g.10383203C>T , CM000681.1:g.10383203C>T | GRCh37 |
| NC_000019.8:g.10244203C>T | NCBI36 |
| NG_012083.1:g.6687C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000264832.8:c.67+1301C>T (ICAM1) MANE Select | ENSP00000264832.2:n.67+1301C>T | |
| ENST00000264832.7:c.67+1301C>T (ICAM1) | ENSP00000264832.2:n.67+1301C>T | |
| ENST00000423829.2:c.67+1301C>T (ICAM1) | ENSP00000413124.2:n.67+1301C>T | |
| ENST00000588645.1:c.67+1301C>T (ICAM1) | ENSP00000465680.1:n.67+1301C>T | |
| NM_000201.2:c.67+1301C>T (ICAM1) | NP_000192.2:n.67+1301C>T | |
| XR_936313.1:n.155-5733G>A (LIMASI) | ||
| XR_936314.1:n.155-5733G>A (LIMASI) | ||
| NM_000201.3:c.67+1301C>T (ICAM1) MANE Select | NP_000192.2:n.67+1301C>T |