Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.69350192T>C , CM000674.2:g.69350192T>C | GRCh38 |
| NC_000012.11:g.69743972T>C , CM000674.1:g.69743972T>C | GRCh37 |
| NC_000012.10:g.68030239T>C | NCBI36 |
| NG_008195.1:g.6839T>C , LRG_768:g.6839T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261267.7:c.221T>C MANE Select | ENSP00000261267.2:p.Ile74Thr | |
| ENST00000261267.6:c.221T>C | ENSP00000261267.2:p.Ile74Thr | |
| ENST00000548839.1:c.221T>C | ENSP00000449969.1:p.Ile74Thr | |
| ENST00000549690.1:c.221T>C | ENSP00000449898.1:p.Ile74Thr | |
| NM_000239.2:c.221T>C , LRG_768t1:c.221T>C | NP_000230.1:p.Ile74Thr | |
| NM_000239.3:c.221T>C MANE Select | NP_000230.1:p.Ile74Thr |