Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.20188918A= , CM000675.2:g.20188918A= | GRCh38 |
| NC_000013.10:g.20763057A= , CM000675.1:g.20763057A= | GRCh37 |
| NC_000013.9:g.19661057A= | NCBI36 |
| NG_008358.1:g.9058T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382844.2:c.664T= | ENSP00000372295.1:p.Ser222= | |
| ENST00000382848.5:c.664T= MANE Select | ENSP00000372299.4:p.Ser222= | |
| ENST00000382844.1:c.664T= | ENSP00000372295.1:p.Ser222= | |
| ENST00000382848.4:c.664T= | ENSP00000372299.4:p.Ser222= | |
| NM_004004.5:c.664T= | NP_003995.2:p.Ser222= | |
| XM_011535049.1:c.664T= | XP_011533351.1:p.Ser222= | |
| XM_011535049.2:c.664T= | XP_011533351.1:p.Ser222= | |
| NM_004004.6:c.664T= MANE Select | NP_003995.2:p.Ser222= |