Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94021933A>C , CM000663.2:g.94021933A>C | GRCh38 |
| NC_000001.10:g.94487489A>C , CM000663.1:g.94487489A>C | GRCh37 |
| NC_000001.9:g.94260077A>C | NCBI36 |
| NG_009073.1:g.104217T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.4686T>G MANE Select | ENSP00000359245.3:p.Ile1562Met | |
| ENST00000370225.3:c.4686T>G | ENSP00000359245.3:p.Ile1562Met | |
| ENST00000460514.1:n.180T>G | ||
| ENST00000536513.5:c.1062T>G | ENSP00000439707.2:p.Ile354Met | |
| NM_000350.2:c.4686T>G | NP_000341.2:p.Ile1562Met | |
| NM_000350.3:c.4686T>G MANE Select | NP_000341.2:p.Ile1562Met |