Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.75765136T>C , CM000679.2:g.75765136T>C | GRCh38 |
| NC_000017.10:g.73761217T>C , CM000679.1:g.73761217T>C | GRCh37 |
| NC_000017.9:g.71272812T>C | NCBI36 |
| NG_008079.1:g.5064A>G | |
| NG_008079.2:g.5064A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000154.2:c.1A>G MANE Select | NP_000145.1:p.Met1Val |
| ENST00000588479.6:c.1A>G MANE Select | ENSP00000465930.1:p.Met1Val |
| NM_000154.1:c.1A>G | NP_000145.1:p.Met1Val |
| NM_001381985.1:c.1A>G | NP_001368914.1:p.Met1Val |
| ENST00000225614.6:c.1A>G | ENSP00000225614.1:p.Met1Val |
| ENST00000586244.1:c.1A>G | ENSP00000468288.1:p.Met1Val |
| ENST00000587707.2:c.1A>G | ENSP00000468341.2:p.Met1Val |
| ENST00000588479.5:c.1A>G | ENSP00000465930.1:p.Met1Val |
| ENST00000592494.1:n.22A>G | |
| ENST00000592997.6:c.1A>G | ENSP00000464765.2:p.Met1Val |