Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23417096A= , CM000678.2:g.23417096A= | GRCh38 |
| NC_000016.9:g.23428417A= , CM000678.1:g.23428417A= | GRCh37 |
| NC_000016.8:g.23335918A= | NCBI36 |
| NG_021287.1:g.41096T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000307149.10:c.1163T= MANE Select | ENSP00000305442.5:p.Val388= | |
| ENST00000307149.9:c.1163T= | ENSP00000305442.5:p.Val388= | |
| ENST00000567821.1:n.198T= | ||
| NM_153603.3:c.1163T= | NP_705831.1:p.Val388= | |
| XR_429680.1:n.1379T= | ||
| XM_017023870.1:c.968T= | XP_016879359.1:p.Val323= | |
| XR_002957852.1:n.1384T= | ||
| XR_429680.2:n.1384T= | ||
| NM_153603.4:c.1163T= MANE Select | NP_705831.1:p.Val388= |