Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218812718C= , CM000664.2:g.218812718C= | GRCh38 |
| NC_000002.11:g.219677441C= , CM000664.1:g.219677441C= | GRCh37 |
| NC_000002.10:g.219385685C= | NCBI36 |
| NG_007959.1:g.35970C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258415.9:c.813C= MANE Select | ENSP00000258415.4:p.Tyr271= | |
| ENST00000258415.8:c.813C= | ENSP00000258415.4:p.Tyr271= | |
| ENST00000411688.1:c.531C= | ENSP00000392671.1:p.Tyr177= | |
| ENST00000445971.1:c.*274C= | ENSP00000404945.1:n.*274C= | |
| ENST00000466602.1:n.761C= | ||
| ENST00000494263.5:n.1247C= | ||
| NM_000784.3:c.813C= | NP_000775.1:p.Tyr271= | |
| XM_017003488.2:c.393C= | XP_016858977.1:p.Tyr131= | |
| NM_000784.4:c.813C= MANE Select | NP_000775.1:p.Tyr271= |