Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94025021G>A , CM000663.2:g.94025021G>A | GRCh38 |
| NC_000001.10:g.94490577G>A , CM000663.1:g.94490577G>A | GRCh37 |
| NC_000001.9:g.94263165G>A | NCBI36 |
| NG_009073.1:g.101129C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.4567C>T MANE Select | ENSP00000359245.3:p.Gln1523Ter | |
| ENST00000370225.3:c.4567C>T | ENSP00000359245.3:p.Gln1523Ter | |
| ENST00000460514.1:n.61C>T | ||
| ENST00000536513.5:c.943C>T | ENSP00000439707.2:p.Gln315Ter | |
| NM_000350.2:c.4567C>T | NP_000341.2:p.Gln1523Ter | |
| NM_000350.3:c.4567C>T MANE Select | NP_000341.2:p.Gln1523Ter |