HGVS | Genome Assembly |
---|---|
NC_000019.10:g.10272599dup , CM000681.2:g.10272599dup | GRCh38 |
NC_000019.9:g.10383275dup , CM000681.1:g.10383275dup | GRCh37 |
NC_000019.8:g.10244275dup | NCBI36 |
NG_012083.1:g.6759dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264832.8:c.67+1373dup (ICAM1) MANE Select | ENSP00000264832.2:n.67+1373dup | |
ENST00000264832.7:c.67+1373dup (ICAM1) | ENSP00000264832.2:n.67+1373dup | |
ENST00000423829.2:c.67+1373dup (ICAM1) | ENSP00000413124.2:n.67+1373dup | |
ENST00000588645.1:c.67+1373dup (ICAM1) | ENSP00000465680.1:n.67+1373dup | |
NM_000201.2:c.67+1373dup (ICAM1) | NP_000192.2:n.67+1373dup | |
XR_936313.1:n.155-5805dup (LIMASI) | ||
XR_936314.1:n.155-5805dup (LIMASI) | ||
NM_000201.3:c.67+1373dup (ICAM1) MANE Select | NP_000192.2:n.67+1373dup |