Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.176094645C= , CM000664.2:g.176094645C= | GRCh38 |
| NC_000002.11:g.176959373C= , CM000664.1:g.176959373C= | GRCh37 |
| NC_000002.10:g.176667619C= | NCBI36 |
| NG_008137.1:g.6842C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000523.4:c.947C= MANE Select | NP_000514.2:p.Ser316= |
| ENST00000392539.4:c.947C= MANE Select | ENSP00000376322.3:p.Ser316= |
| NM_000523.3:c.947C= | NP_000514.2:p.Ser316= |
| ENST00000392539.3:c.947C= | ENSP00000376322.3:p.Ser316= |
| XM_011511068.1:c.890C= | XP_011509370.1:p.Ser297= |
| XM_011511068.2:c.890C= | XP_011509370.1:p.Ser297= |