Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.137199369T= , CM000671.2:g.137199369T= | GRCh38 |
| NC_000009.11:g.140093821T= , CM000671.1:g.140093821T= | GRCh37 |
| NC_000009.10:g.139213642T= | NCBI36 |
| NG_027801.1:g.6343A= | |
| NG_027801.2:g.9825A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409012.6:c.1343A= MANE Select | ENSP00000387100.4:p.Tyr448= | |
| ENST00000333046.8:c.737A= | ENSP00000327617.4:p.Tyr246= | |
| ENST00000409012.4:c.1343A= | ENSP00000387100.4:p.Tyr448= | |
| ENST00000541945.1:n.90+4735A= | ||
| NM_001128228.2:c.1343A= | NP_001121700.2:p.Tyr448= | |
| NM_001128228.3:c.1343A= MANE Select | NP_001121700.2:p.Tyr448= |