Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131864886A= , CM000668.2:g.131864886A= | GRCh38 |
| NC_000006.11:g.132186026A= , CM000668.1:g.132186026A= | GRCh37 |
| NC_000006.10:g.132227719A= | NCBI36 |
| NG_008206.1:g.61871A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006208.3:c.1112A= MANE Select | NP_006199.2:p.Tyr371= |
| ENST00000647893.1:c.1112A= MANE Select | ENSP00000498074.1:p.Tyr371= |
| NM_006208.2:c.1112A= | NP_006199.2:p.Tyr371= |
| ENST00000360971.6:c.1112A= | ENSP00000354238.2:p.Tyr371= |
| ENST00000459624.1:n.162-6A= | |
| ENST00000513998.5:c.1092-6A= | ENSP00000422424.1:n.1092-6A= |
| ENST00000650147.1:c.1023A= | |
| ENST00000650437.1:c.603A= | |
| XM_011535896.1:c.8-6A= | XP_011534198.1:n.8-6A= |