Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.40847036A>T , CM000681.2:g.40847036A>T | GRCh38 |
| NC_000019.9:g.41352941A>T , CM000681.1:g.41352941A>T | GRCh37 |
| NC_000019.8:g.46044781A>T | NCBI36 |
| NG_008377.1:g.8412T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000762.6:c.670T>A MANE Select | NP_000753.3:p.Ser224Thr |
| ENST00000301141.10:c.670T>A MANE Select | ENSP00000301141.4:p.Ser224Thr |
| NM_000762.5:c.670T>A | NP_000753.3:p.Ser224Thr |
| ENST00000301141.9:c.670T>A | ENSP00000301141.4:p.Ser224Thr |
| ENST00000596719.5:n.521T>A | |
| ENST00000600495.1:c.*482T>A | ENSP00000472905.1:n.*482T>A |
| ENST00000601627.1:c.120-44955A>T | |
| ENST00000610301.1:c.670T>A | ENSP00000477899.1:p.Ser224Thr |