Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.67009142A>G , CM000663.2:g.67009142A>G | GRCh38 |
| NC_000001.10:g.67474825A>G , CM000663.1:g.67474825A>G | GRCh37 |
| NC_000001.9:g.67247413A>G | NCBI36 |
| NG_012933.1:g.50256T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_015139.3:c.902T>C MANE Select | NP_055954.1:p.Met301Thr |
| ENST00000235345.6:c.902T>C MANE Select | ENSP00000235345.5:p.Met301Thr |
| NM_015139.2:c.902T>C | NP_055954.1:p.Met301Thr |
| ENST00000235345.5:c.902T>C | ENSP00000235345.5:p.Met301Thr |
| XM_006710478.1:c.983T>C | XP_006710541.1:p.Met328Thr |
| XM_006710478.2:c.983T>C | XP_006710541.1:p.Met328Thr |
| XM_011541070.1:c.983T>C | XP_011539372.1:p.Met328Thr |
| XM_011541070.2:c.983T>C | XP_011539372.1:p.Met328Thr |
| XR_001737057.2:n.1486T>C | |
| XR_001737058.2:n.2271T>C |