Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4911902T>C , CM000674.2:g.4911902T>C | GRCh38 |
| NC_000012.11:g.5021068T>C , CM000674.1:g.5021068T>C | GRCh37 |
| NC_000012.10:g.4891329T>C | NCBI36 |
| NG_011815.1:g.6996T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.524T>C MANE Select | ENSP00000371985.3:p.Met175Thr | |
| ENST00000543874.3:n.105+1430T>C | ||
| ENST00000639306.1:c.362T>C | ENSP00000492506.1:p.Met121Thr | |
| ENST00000382545.3:c.524T>C | ENSP00000371985.3:p.Met175Thr | |
| ENST00000541095.1:n.105+1430T>C | ||
| ENST00000543874.2:n.96+1430T>C | ||
| NM_000217.2:c.524T>C | NP_000208.2:p.Met175Thr | |
| NM_000217.3:c.524T>C MANE Select | NP_000208.2:p.Met175Thr |