HGVS | Genome Assembly |
---|---|
NC_000006.12:g.1610843_1610846del , CM000668.2:g.1610843_1610846del | GRCh38 |
NC_000006.11:g.1611078_1611081del , CM000668.1:g.1611078_1611081del | GRCh37 |
NC_000006.10:g.1556077_1556080del | NCBI36 |
NG_009368.1:g.5398_5401del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645831.2:c.398_401del MANE Select | ENSP00000493906.1:p.Asn133SerfsTer? | |
ENST00000380874.3:c.398_401del | ENSP00000370256.2:p.Asn133SerfsTer? | |
NM_001453.2:c.398_401del | NP_001444.2:p.Asn133SerfsTer? | |
NM_001453.3:c.398_401del MANE Select | NP_001444.2:p.Asn133SerfsTer? |