Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44374760T= , CM000679.2:g.44374760T= | GRCh38 |
| NC_000017.10:g.42452128T= , CM000679.1:g.42452128T= | GRCh37 |
| NC_000017.9:g.39807654T= | NCBI36 |
| NG_008331.1:g.19746A= , LRG_479:g.19746A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262407.6:c.2842A= MANE Select | ENSP00000262407.5:p.Arg948= | |
| ENST00000648408.1:c.2273A= | ||
| ENST00000262407.5:c.2842A= | ENSP00000262407.5:p.Arg948= | |
| ENST00000587295.5:c.253+1073A= | ||
| ENST00000592462.5:n.2353A= | ||
| NM_000419.3:c.2842A= , LRG_479t1:c.2842A= | NP_000410.2:p.Arg948= | |
| XM_011524749.1:c.2841+238A= | XP_011523051.1:n.2841+238A= | |
| XM_011524750.1:c.2842A= | XP_011523052.1:p.Arg948= | |
| NM_000419.4:c.2842A= | NP_000410.2:p.Arg948= | |
| NM_000419.5:c.2842A= MANE Select | NP_000410.2:p.Arg948= |