Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.29480264T>C , CM000684.2:g.29480264T>C | GRCh38 |
| NC_000022.10:g.29876253T>C , CM000684.1:g.29876253T>C | GRCh37 |
| NC_000022.9:g.28206253T>C | NCBI36 |
| NG_008404.1:g.5073T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000310624.7:c.2T>C MANE Select | ENSP00000311997.6:p.Met1Thr | |
| ENST00000310624.6:c.2T>C | ENSP00000311997.6:p.Met1Thr | |
| NM_021076.3:c.2T>C | NP_066554.2:p.Met1Thr | |
| XM_011530200.1:c.2T>C | XP_011528502.1:p.Met1Thr | |
| XM_011530200.2:c.2T>C | XP_011528502.1:p.Met1Thr | |
| NM_021076.4:c.2T>C MANE Select | NP_066554.2:p.Met1Thr |