Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.14139243T= , CM000665.2:g.14139243T= | GRCh38 |
| NC_000003.11:g.14180743T= , CM000665.1:g.14180743T= | GRCh37 |
| NC_000003.10:g.14155744T= | NCBI36 |
| NG_008975.1:g.19304T= , LRG_435:g.19304T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000432444.2:c.*976T= | ENSP00000395617.1:n.*976T= | |
| ENST00000306077.5:c.946T= MANE Select | ENSP00000303992.5:p.Trp316= | |
| ENST00000306077.4:c.946T= | ENSP00000303992.4:p.Trp316= | |
| ENST00000601399.3:n.273T= | ||
| ENST00000608606.1:c.182T= | ||
| NM_024334.2:c.946T= , LRG_435t1:c.946T= | NP_077310.1:p.Trp316= | |
| XM_011534109.1:c.841T= | XP_011532411.1:p.Trp281= | |
| XM_017007176.2:c.841T= | XP_016862665.1:p.Trp281= | |
| NM_024334.3:c.946T= MANE Select | NP_077310.1:p.Trp316= |