Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232541457T>C , CM000664.2:g.232541457T>C | GRCh38 |
| NC_000002.11:g.233406167T>C , CM000664.1:g.233406167T>C | GRCh37 |
| NC_000002.10:g.233114411T>C | NCBI36 |
| NG_012954.1:g.6731T>C | |
| NG_012954.2:g.6766T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651502.1:c.434T>C MANE Select | ENSP00000498757.1:p.Ile145Thr | |
| ENST00000389492.3:c.350+746T>C | ENSP00000374143.3:n.350+746T>C | |
| ENST00000389494.7:c.434T>C | ENSP00000374145.3:p.Ile145Thr | |
| ENST00000485094.1:n.455T>C | ||
| NM_005199.4:c.434T>C | NP_005190.4:p.Ile145Thr | |
| NM_005199.5:c.434T>C MANE Select | NP_005190.4:p.Ile145Thr |