Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.46853807T>C , CM000685.2:g.46853807T>C | GRCh38 |
| NC_000023.10:g.46713242T>C , CM000685.1:g.46713242T>C | GRCh37 |
| NC_000023.9:g.46598186T>C | NCBI36 |
| NG_009107.1:g.21896T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006915.3:c.434T>C MANE Select | NP_008846.2:p.Phe145Ser |
| ENST00000218340.4:c.434T>C MANE Select | ENSP00000218340.3:p.Phe145Ser |
| NM_006915.2:c.434T>C | NP_008846.2:p.Phe145Ser |
| ENST00000218340.3:c.434T>C | ENSP00000218340.3:p.Phe145Ser |