Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131890435A= , CM000668.2:g.131890435A= | GRCh38 |
| NC_000006.11:g.132211575A= , CM000668.1:g.132211575A= | GRCh37 |
| NC_000006.10:g.132253268A= | NCBI36 |
| NG_008206.1:g.87420A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006208.3:c.2702A= MANE Select | NP_006199.2:p.Tyr901= |
| ENST00000647893.1:c.2702A= MANE Select | ENSP00000498074.1:p.Tyr901= |
| NM_006208.2:c.2702A= | NP_006199.2:p.Tyr901= |
| ENST00000360971.6:c.2702A= | ENSP00000354238.2:p.Tyr901= |
| ENST00000513998.5:c.*1539A= | ENSP00000422424.1:n.*1539A= |
| ENST00000684674.1:n.1133A= | |
| XM_011535896.1:c.1592A= | XP_011534198.1:p.Tyr531= |