Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19951783T>C , CM000670.2:g.19951783T>C | GRCh38 |
| NC_000008.10:g.19809294T>C , CM000670.1:g.19809294T>C | GRCh37 |
| NC_000008.9:g.19853574T>C | NCBI36 |
| NG_008855.1:g.17713T>C | |
| NG_008855.2:g.55067T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000237.3:c.264T>C MANE Select | NP_000228.1:p.Tyr88= |
| ENST00000650287.1:c.264T>C MANE Select | ENSP00000497642.1:p.Tyr88= |
| NM_000237.2:c.264T>C | NP_000228.1:p.Tyr88= |
| ENST00000311322.8:c.264T>C | ENSP00000309757.6:p.Tyr88= |
| ENST00000520959.5:c.36T>C | ENSP00000428496.1:p.Tyr12= |
| ENST00000521994.1:n.521T>C | |
| ENST00000522701.5:c.264T>C | ENSP00000428557.1:p.Tyr88= |
| ENST00000524029.5:c.264T>C | ENSP00000428237.1:p.Tyr88= |