Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119415089A= , CM000665.2:g.119415089A= | GRCh38 |
| NC_000003.11:g.119133936A= , CM000665.1:g.119133936A= | GRCh37 |
| NC_000003.10:g.120616626A= | NCBI36 |
| NG_007665.2:g.125717A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.3160A= MANE Select | ENSP00000264245.4:p.Ser1054= | |
| ENST00000264245.8:c.3160A= | ENSP00000264245.4:p.Ser1054= | |
| NM_020754.3:c.3160A= | NP_065805.2:p.Ser1054= | |
| XM_005247671.3:c.3067A= | XP_005247728.1:p.Ser1023= | |
| XM_006713714.2:c.3100A= | XP_006713777.1:p.Ser1034= | |
| XM_006713714.3:c.3100A= | XP_006713777.1:p.Ser1034= | |
| XM_017006955.1:c.2668A= | XP_016862444.1:p.Ser890= | |
| NM_020754.4:c.3160A= MANE Select | NP_065805.2:p.Ser1054= |