Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154999482T>C , CM000685.2:g.154999482T>C | GRCh38 |
| NC_000023.10:g.154227757T>C , CM000685.1:g.154227757T>C | GRCh37 |
| NC_000023.9:g.153880951T>C | NCBI36 |
| NG_011403.1:g.28242A>G | |
| NG_011403.2:g.28242A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.262A>G MANE Select | NP_000123.1:p.Met88Val |
| ENST00000360256.9:c.262A>G MANE Select | ENSP00000353393.4:p.Met88Val |
| NM_000132.3:c.262A>G | NP_000123.1:p.Met88Val |
| ENST00000360256.8:c.262A>G | ENSP00000353393.4:p.Met88Val |
| ENST00000423959.5:c.157A>G | ENSP00000409446.1:p.Met53Val |
| ENST00000453950.1:c.244A>G | ENSP00000389153.1:p.Met82Val |
| ENST00000647125.1:c.*48A>G | ENSP00000496062.1:n.*48A>G |
| XM_011531126.1:c.157A>G | XP_011529428.1:p.Met53Val |