Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.87016119C= , CM000668.2:g.87016119C= | GRCh38 |
| NC_000006.11:g.87725837C= , CM000668.1:g.87725837C= | GRCh37 |
| NC_000006.10:g.87782556C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000865.3:c.785C= MANE Select | NP_000856.1:p.Ser262= |
| ENST00000305344.7:c.785C= MANE Select | ENSP00000307766.4:p.Ser262= |
| NM_000865.2:c.785C= | NP_000856.1:p.Ser262= |
| ENST00000305344.6:c.785C= | ENSP00000307766.4:p.Ser262= |
| XM_011535789.1:c.785C= | XP_011534091.1:p.Ser262= |
| XM_011535789.2:c.785C= | XP_011534091.1:p.Ser262= |
| XM_011535790.1:c.785C= | XP_011534092.1:p.Ser262= |