Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.14130916G= , CM000665.2:g.14130916G= | GRCh38 |
| NC_000003.11:g.14172416G= , CM000665.1:g.14172416G= | GRCh37 |
| NC_000003.10:g.14147417G= | NCBI36 |
| NG_008975.1:g.10977G= , LRG_435:g.10977G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000432444.2:c.*287G= | ENSP00000395617.1:n.*287G= | |
| ENST00000306077.5:c.257G= MANE Select | ENSP00000303992.5:p.Gly86= | |
| ENST00000306077.4:c.257G= | ENSP00000303992.4:p.Gly86= | |
| ENST00000432444.1:c.*287G= | ENSP00000395617.1:n.*287G= | |
| NM_024334.2:c.257G= , LRG_435t1:c.257G= | NP_077310.1:p.Gly86= | |
| XM_011534109.1:c.152G= | XP_011532411.1:p.Gly51= | |
| XM_017007176.2:c.152G= | XP_016862665.1:p.Gly51= | |
| NM_024334.3:c.257G= MANE Select | NP_077310.1:p.Gly86= |