Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.5006947G>A , CM000679.2:g.5006947G>A | GRCh38 |
| NC_000017.10:g.4910242G>A , CM000679.1:g.4910242G>A | GRCh37 |
| NC_000017.9:g.4850966G>A | NCBI36 |
| NG_034137.1:g.14000G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006612.6:c.1198G>A MANE Select | NP_006603.2:p.Ala400Thr |
| ENST00000320785.10:c.1198G>A MANE Select | ENSP00000320821.5:p.Ala400Thr |
| NM_006612.5:c.1198G>A | NP_006603.2:p.Ala400Thr |
| ENST00000320785.9:c.1198G>A | ENSP00000320821.5:p.Ala400Thr |
| XM_005256424.1:c.1198G>A | XP_005256481.1:p.Ala400Thr |
| XM_005256424.2:c.1198G>A | XP_005256481.1:p.Ala400Thr |