Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4372632A= , CM000674.2:g.4372632A= | GRCh38 |
| NC_000012.11:g.4481798A= , CM000674.1:g.4481798A= | GRCh37 |
| NC_000012.10:g.4352059A= | NCBI36 |
| NG_007087.1:g.12097T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000237837.2:c.277T= MANE Select | ENSP00000237837.1:p.Tyr93= | |
| ENST00000648100.1:c.*1967+6350A= | ENSP00000497536.1:n.*1967+6350A= | |
| ENST00000648269.1:n.1777T= | ||
| ENST00000674624.1:c.*1204+6350A= | ENSP00000501898.1:n.*1204+6350A= | |
| ENST00000237837.1:c.277T= | ENSP00000237837.1:p.Tyr93= | |
| NM_020638.2:c.277T= | NP_065689.1:p.Tyr93= | |
| NM_020638.3:c.277T= MANE Select | NP_065689.1:p.Tyr93= |