Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229432311A>G , CM000663.2:g.229432311A>G | GRCh38 |
| NC_000001.10:g.229568058A>G , CM000663.1:g.229568058A>G | GRCh37 |
| NC_000001.9:g.227634681A>G | NCBI36 |
| NG_006672.1:g.6786T>C , LRG_429:g.6786T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366683.4:c.575T>C | ENSP00000355644.4:p.Met192Thr | |
| ENST00000684723.1:c.440T>C | ENSP00000508084.1:p.Met147Thr | |
| ENST00000366683.3:c.479+96T>C | ENSP00000355644.3:n.479+96T>C | |
| ENST00000366684.7:c.575T>C MANE Select | ENSP00000355645.3:p.Met192Thr | |
| NM_001100.3:c.575T>C , LRG_429t1:c.575T>C | NP_001091.1:p.Met192Thr | |
| NM_001100.4:c.575T>C MANE Select | NP_001091.1:p.Met192Thr |