Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.1610897A= , CM000668.2:g.1610897A= | GRCh38 |
| NC_000006.11:g.1611132A= , CM000668.1:g.1611132A= | GRCh37 |
| NC_000006.10:g.1556131A= | NCBI36 |
| NG_009368.1:g.5452A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645831.2:c.452A= MANE Select | ENSP00000493906.1:p.Tyr151= | |
| ENST00000380874.3:c.452A= | ENSP00000370256.2:p.Tyr151= | |
| NM_001453.2:c.452A= | NP_001444.2:p.Tyr151= | |
| NM_001453.3:c.452A= MANE Select | NP_001444.2:p.Tyr151= |