Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.56042168T>C , CM000674.2:g.56042168T>C | GRCh38 |
| NC_000012.11:g.56435952T>C , CM000674.1:g.56435952T>C | GRCh37 |
| NC_000012.10:g.54722219T>C | NCBI36 |
| NG_023201.1:g.5267T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001029.5:c.2T>C MANE Select | NP_001020.2:p.Met1Thr |
| ENST00000646449.2:c.2T>C MANE Select | ENSP00000496643.1:p.Met1Thr |
| NM_001029.3:c.2T>C | NP_001020.2:p.Met1Thr |
| ENST00000356464.10:c.2T>C | ENSP00000348849.5:p.Met1Thr |
| ENST00000356464.9:c.2T>C | ENSP00000348849.5:p.Met1Thr |
| ENST00000548590.1:n.29T>C | |
| ENST00000552361.1:c.2T>C | ENSP00000450339.1:p.Met1Thr |