Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23417093T= , CM000678.2:g.23417093T= | GRCh38 |
| NC_000016.9:g.23428414T= , CM000678.1:g.23428414T= | GRCh37 |
| NC_000016.8:g.23335915T= | NCBI36 |
| NG_021287.1:g.41099A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307149.10:c.1166A= MANE Select | ENSP00000305442.5:p.Gln389= | |
| ENST00000307149.9:c.1166A= | ENSP00000305442.5:p.Gln389= | |
| ENST00000567821.1:n.201A= | ||
| NM_153603.3:c.1166A= | NP_705831.1:p.Gln389= | |
| XR_429680.1:n.1382A= | ||
| XM_017023870.1:c.971A= | XP_016879359.1:p.Gln324= | |
| XR_002957852.1:n.1387A= | ||
| XR_429680.2:n.1387A= | ||
| NM_153603.4:c.1166A= MANE Select | NP_705831.1:p.Gln389= |