Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119916415A>T , CM000663.2:g.119916415A>T | GRCh38 |
| NC_000001.10:g.120459038A>T , CM000663.1:g.120459038A>T | GRCh37 |
| NC_000001.9:g.120260561A>T | NCBI36 |
| NG_008163.1:g.158239T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_024408.4:c.6307T>A MANE Select | NP_077719.2:p.Ser2103Thr |
| ENST00000256646.7:c.6307T>A MANE Select | ENSP00000256646.2:p.Ser2103Thr |
| NM_024408.3:c.6307T>A | NP_077719.2:p.Ser2103Thr |
| ENST00000256646.6:c.6307T>A | ENSP00000256646.2:p.Ser2103Thr |
| XM_005270901.2:c.6190T>A | XP_005270958.1:p.Ser2064Thr |
| XM_011541519.1:c.6295T>A | XP_011539821.1:p.Ser2099Thr |
| XM_011541520.1:c.6190T>A | XP_011539822.1:p.Ser2064Thr |