Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10412931A>G , CM000682.2:g.10412931A>G | GRCh38 |
| NC_000020.10:g.10393579A>G , CM000682.1:g.10393579A>G | GRCh37 |
| NC_000020.9:g.10341579A>G | NCBI36 |
| NG_009109.1:g.26288T>C | |
| NG_009109.2:g.26288T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651692.1:c.584T>C | ENSP00000498849.1:p.Ile195Thr | |
| ENST00000652676.1:n.459-231T>C | ||
| ENST00000347364.7:c.584T>C MANE Select | ENSP00000246062.4:p.Ile195Thr | |
| ENST00000399054.6:c.584T>C | ENSP00000382008.2:p.Ile195Thr | |
| NM_018848.3:c.584T>C | NP_061336.1:p.Ile195Thr | |
| NM_170784.2:c.584T>C | NP_740754.1:p.Ile195Thr | |
| NR_072977.1:n.364-4128T>C | ||
| NR_072977.2:n.347-4128T>C | ||
| NM_170784.3:c.584T>C MANE Select | NP_740754.1:p.Ile195Thr |