Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25012998T>A , CM000685.2:g.25012998T>A | GRCh38 |
| NC_000023.10:g.25031115T>A , CM000685.1:g.25031115T>A | GRCh37 |
| NC_000023.9:g.24941036T>A | NCBI36 |
| NG_008281.1:g.7951A>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_139058.3:c.997A>T MANE Select | NP_620689.1:p.Thr333Ser |
| ENST00000379044.5:c.997A>T MANE Select | ENSP00000368332.4:p.Thr333Ser |
| NM_139058.2:c.997A>T | NP_620689.1:p.Thr333Ser |
| ENST00000379044.4:c.997A>T | ENSP00000368332.4:p.Thr333Ser |