Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94043445A>C , CM000663.2:g.94043445A>C | GRCh38 |
| NC_000001.10:g.94509001A>C , CM000663.1:g.94509001A>C | GRCh37 |
| NC_000001.9:g.94281589A>C | NCBI36 |
| NG_009073.1:g.82705T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.3081T>G MANE Select | NP_000341.2:p.Tyr1027Ter |
| ENST00000370225.4:c.3081T>G MANE Select | ENSP00000359245.3:p.Tyr1027Ter |
| NM_000350.2:c.3081T>G | NP_000341.2:p.Tyr1027Ter |
| ENST00000370225.3:c.3081T>G | ENSP00000359245.3:p.Tyr1027Ter |
| ENST00000536513.5:c.-64-3356T>G | ENSP00000439707.2:n.-64-3356T>G |