gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.69022677 (AFR)
Genomes Max Group AF
0.69022677 (AFR)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10279982C>G , CM000681.2:g.10279982C>G | GRCh38 |
| NC_000019.9:g.10390658C>G , CM000681.1:g.10390658C>G | GRCh37 |
| NC_000019.8:g.10251658C>G | NCBI36 |
| NG_012083.1:g.14142C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264832.8:c.332-3499C>G (ICAM1) MANE Select | ENSP00000264832.2:n.332-3499C>G | |
| ENST00000264832.7:c.332-3499C>G (ICAM1) | ENSP00000264832.2:n.332-3499C>G | |
| ENST00000423829.2:c.68-4147C>G (ICAM1) | ENSP00000413124.2:n.68-4147C>G | |
| ENST00000588645.1:c.332-3499C>G (ICAM1) | ENSP00000465680.1:n.332-3499C>G | |
| NM_000201.2:c.332-3499C>G (ICAM1) | NP_000192.2:n.332-3499C>G | |
| XR_936313.1:n.154+3339G>C (LIMASI) | ||
| XR_936314.1:n.154+3339G>C (LIMASI) | ||
| NM_000201.3:c.332-3499C>G (ICAM1) MANE Select | NP_000192.2:n.332-3499C>G |