HGVS | Genome Assembly |
---|---|
NC_000019.10:g.10272577T>C , CM000681.2:g.10272577T>C | GRCh38 |
NC_000019.9:g.10383253T>C , CM000681.1:g.10383253T>C | GRCh37 |
NC_000019.8:g.10244253T>C | NCBI36 |
NG_012083.1:g.6737T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264832.8:c.67+1351T>C (ICAM1) MANE Select | ENSP00000264832.2:n.67+1351T>C | |
ENST00000264832.7:c.67+1351T>C (ICAM1) | ENSP00000264832.2:n.67+1351T>C | |
ENST00000423829.2:c.67+1351T>C (ICAM1) | ENSP00000413124.2:n.67+1351T>C | |
ENST00000588645.1:c.67+1351T>C (ICAM1) | ENSP00000465680.1:n.67+1351T>C | |
NM_000201.2:c.67+1351T>C (ICAM1) | NP_000192.2:n.67+1351T>C | |
XR_936313.1:n.155-5783A>G (LIMASI) | ||
XR_936314.1:n.155-5783A>G (LIMASI) | ||
NM_000201.3:c.67+1351T>C (ICAM1) MANE Select | NP_000192.2:n.67+1351T>C |