HGVS | Genome Assembly |
---|---|
NC_000019.10:g.10272592T>G , CM000681.2:g.10272592T>G | GRCh38 |
NC_000019.9:g.10383268T>G , CM000681.1:g.10383268T>G | GRCh37 |
NC_000019.8:g.10244268T>G | NCBI36 |
NG_012083.1:g.6752T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264832.8:c.67+1366T>G (ICAM1) MANE Select | ENSP00000264832.2:n.67+1366T>G | |
ENST00000264832.7:c.67+1366T>G (ICAM1) | ENSP00000264832.2:n.67+1366T>G | |
ENST00000423829.2:c.67+1366T>G (ICAM1) | ENSP00000413124.2:n.67+1366T>G | |
ENST00000588645.1:c.67+1366T>G (ICAM1) | ENSP00000465680.1:n.67+1366T>G | |
NM_000201.2:c.67+1366T>G (ICAM1) | NP_000192.2:n.67+1366T>G | |
XR_936313.1:n.155-5798A>C (LIMASI) | ||
XR_936314.1:n.155-5798A>C (LIMASI) | ||
NM_000201.3:c.67+1366T>G (ICAM1) MANE Select | NP_000192.2:n.67+1366T>G |