Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.48530455C>G , CM000679.2:g.48530455C>G | GRCh38 |
| NC_000017.10:g.46607817C>G , CM000679.1:g.46607817C>G | GRCh37 |
| NC_000017.9:g.43962816C>G | NCBI36 |
| NG_032884.1:g.5456G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002144.4:c.450G>C MANE Select | NP_002135.2:p.Ala150= |
| ENST00000239174.7:c.450G>C MANE Select | ENSP00000355140.5:p.Ala150= |
| NM_002144.3:c.450G>C | NP_002135.2:p.Ala150= |
| ENST00000239174.6:c.450G>C | ENSP00000355140.5:p.Ala150= |
| ENST00000577092.1:c.450G>C | ENSP00000459066.1:p.Ala150= |