Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.49622073T= , CM000676.2:g.49622073T= | GRCh38 |
| NC_000014.8:g.50088791T= , CM000676.1:g.50088791T= | GRCh37 |
| NC_000014.7:g.49158541T= | NCBI36 |
| NG_008920.1:g.6303T= | |
| NG_033054.1:g.3559A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305386.4:c.805T= MANE Select | ENSP00000307423.2:p.Tyr269= | |
| ENST00000305386.3:c.805T= | ENSP00000307423.2:p.Tyr269= | |
| NM_002408.3:c.805T= | NP_002399.1:p.Tyr269= | |
| NM_002408.4:c.805T= MANE Select | NP_002399.1:p.Tyr269= |