Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.44275530G>A , CM000673.2:g.44275530G>A | GRCh38 |
| NC_000011.9:g.44297080G>A , CM000673.1:g.44297080G>A | GRCh37 |
| NC_000011.8:g.44253656G>A | NCBI36 |
| NG_015809.1:g.39637C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000652299.1:c.595C>T MANE Select | ENSP00000498217.1:p.Pro199Ser | |
| ENST00000329255.3:c.595C>T | ENSP00000332744.3:p.Pro199Ser | |
| NM_021926.3:c.595C>T | NP_068745.2:p.Pro199Ser | |
| XM_011520264.1:c.595C>T | XP_011518566.1:p.Pro199Ser | |
| XM_011520265.1:c.73C>T | XP_011518567.1:p.Pro25Ser | |
| XM_011520266.1:c.73C>T | XP_011518568.1:p.Pro25Ser | |
| NM_021926.4:c.595C>T MANE Select | NP_068745.2:p.Pro199Ser |