Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154947710T>C , CM000685.2:g.154947710T>C | GRCh38 |
| NC_000023.10:g.154175985T>C , CM000685.1:g.154175985T>C | GRCh37 |
| NC_000023.9:g.153829179T>C | NCBI36 |
| NG_011403.1:g.80014A>G | |
| NG_011403.2:g.80014A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.2101A>G MANE Select | NP_000123.1:p.Met701Val |
| ENST00000360256.9:c.2101A>G MANE Select | ENSP00000353393.4:p.Met701Val |
| NM_000132.3:c.2101A>G | NP_000123.1:p.Met701Val |
| ENST00000360256.8:c.2101A>G | ENSP00000353393.4:p.Met701Val |
| ENST00000647125.1:c.*1779+6182A>G | ENSP00000496062.1:n.*1779+6182A>G |
| XM_011531126.1:c.1996A>G | XP_011529428.1:p.Met666Val |