Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.216122160T>C , CM000664.2:g.216122160T>C | GRCh38 |
| NC_000002.11:g.216986883T>C , CM000664.1:g.216986883T>C | GRCh37 |
| NC_000002.10:g.216695128T>C | NCBI36 |
| NG_029780.1:g.17864T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392132.7:c.590T>C MANE Select | ENSP00000375977.2:p.Ile197Thr | |
| ENST00000392132.6:c.590T>C | ENSP00000375977.2:p.Ile197Thr | |
| ENST00000392133.7:c.590T>C | ENSP00000375978.3:p.Ile197Thr | |
| ENST00000460284.5:n.1132T>C | ||
| NM_021141.3:c.590T>C | NP_066964.1:p.Ile197Thr | |
| NM_021141.4:c.590T>C MANE Select | NP_066964.1:p.Ile197Thr |