Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.97584820C>T , CM000672.2:g.97584820C>T | GRCh38 |
| NC_000010.10:g.99344577C>T , CM000672.1:g.99344577C>T | GRCh37 |
| NC_000010.9:g.99334567C>T | NCBI36 |
| NG_027922.1:g.5476C>T | |
| NG_034079.1:g.17380C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370646.9:c.117C>T MANE Select | ENSP00000359680.4:p.Tyr39= | |
| ENST00000370646.8:c.117C>T | ENSP00000359680.4:p.Tyr39= | |
| ENST00000370647.8:c.117C>T | ENSP00000359681.4:p.Tyr39= | |
| ENST00000370649.3:c.117C>T | ENSP00000359683.3:p.Tyr39= | |
| ENST00000465608.1:n.498C>T | ||
| NM_001134670.1:c.117C>T | NP_001128142.1:p.Tyr39= | |
| NM_138413.3:c.117C>T | NP_612422.2:p.Tyr39= | |
| NM_138413.4:c.117C>T MANE Select | NP_612422.2:p.Tyr39= | |
| NM_001134670.2:c.117C>T | NP_001128142.1:p.Tyr39= |