Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10115505G>A , CM000681.2:g.10115505G>A | GRCh38 |
| NC_000019.9:g.10226181G>A , CM000681.1:g.10226181G>A | GRCh37 |
| NC_000019.8:g.10087181G>A | NCBI36 |
| NG_047007.1:g.8985G>A | |
| NG_051197.1:g.9420C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253108.9:c.921C>T MANE Select | ENSP00000253108.3:p.His307= | |
| ENST00000253108.8:c.921C>T | ENSP00000253108.3:p.His307= | |
| ENST00000590158.1:n.940C>T | ||
| ENST00000593054.5:c.315C>T | ENSP00000467187.1:p.His105= | |
| NM_003755.3:c.921C>T | NP_003746.2:p.His307= | |
| NM_003755.4:c.921C>T | NP_003746.2:p.His307= | |
| NM_003755.5:c.921C>T MANE Select | NP_003746.2:p.His307= |