Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270375C>A , CM000668.2:g.31270375C>A | GRCh38 |
| NC_000006.11:g.31238152C>A , CM000668.1:g.31238152C>A | GRCh37 |
| NC_000006.10:g.31346131C>A | NCBI36 |
| NG_029422.2:g.6757G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.730G>T MANE Select | ENSP00000365402.5:p.Asp244Tyr | |
| ENST00000376228.9:c.730G>T | ENSP00000365402.5:p.Asp244Tyr | |
| ENST00000376237.8:c.*317G>T | ENSP00000365412.4:n.*317G>T | |
| ENST00000383329.7:c.730G>T | ENSP00000372819.3:p.Asp244Tyr | |
| ENST00000415537.1:c.665-44G>T | ||
| ENST00000470363.5:n.48G>T | ||
| ENST00000487245.5:n.1089G>T | ||
| ENST00000495835.1:n.919G>T | ||
| NM_002117.5:c.730G>T | NP_002108.4:p.Asp244Tyr | |
| NM_002117.6:c.730G>T MANE Select | NP_002108.4:p.Asp244Tyr |