Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154957055A= , CM000685.2:g.154957055A= | GRCh38 |
| NC_000023.10:g.154185330A= , CM000685.1:g.154185330A= | GRCh37 |
| NC_000023.9:g.153838524A= | NCBI36 |
| NG_011403.1:g.70669T= | |
| NG_011403.2:g.70669T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.1654T= MANE Select | ENSP00000353393.4:p.Tyr552= | |
| ENST00000647125.1:c.*1530T= | ENSP00000496062.1:n.*1530T= | |
| ENST00000360256.8:c.1654T= | ENSP00000353393.4:p.Tyr552= | |
| NM_000132.3:c.1654T= | NP_000123.1:p.Tyr552= | |
| XM_011531126.1:c.1549T= | XP_011529428.1:p.Tyr517= | |
| NM_000132.4:c.1654T= MANE Select | NP_000123.1:p.Tyr552= |