Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102955342A>G , CM000673.2:g.102955342A>G | GRCh38 |
| NC_000011.9:g.102826071A>G , CM000673.1:g.102826071A>G | GRCh37 |
| NC_000011.8:g.102331281A>G | NCBI36 |
| NG_021404.1:g.5393T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000260302.8:c.272T>C MANE Select | ENSP00000260302.3:p.Met91Thr | |
| ENST00000260302.7:c.272T>C | ENSP00000260302.3:p.Met91Thr | |
| ENST00000340273.4:c.272T>C | ENSP00000339672.4:p.Met91Thr | |
| ENST00000615555.4:c.272T>C | ENSP00000482883.1:p.Met91Thr | |
| NM_002427.3:c.272T>C | NP_002418.1:p.Met91Thr | |
| NM_002427.4:c.272T>C MANE Select | NP_002418.1:p.Met91Thr |