Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.130862898T>A , CM000671.2:g.130862898T>A | GRCh38 |
| NC_000009.11:g.133738285T>A , CM000671.1:g.133738285T>A | GRCh37 |
| NC_000009.10:g.132728106T>A | NCBI36 |
| NG_012034.1:g.154018T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372348.9:c.742T>A | ENSP00000361423.2:p.Ser248Thr | |
| ENST00000318560.6:c.685T>A MANE Select | ENSP00000323315.5:p.Ser229Thr | |
| ENST00000372348.7:c.742T>A | ENSP00000361423.2:p.Ser248Thr | |
| ENST00000318560.5:c.685T>A | ENSP00000323315.5:p.Ser229Thr | |
| ENST00000372348.6:c.742T>A | ENSP00000361423.2:p.Ser248Thr | |
| NM_005157.5:c.685T>A | NP_005148.2:p.Ser229Thr | |
| NM_007313.2:c.742T>A | NP_009297.2:p.Ser248Thr | |
| NM_005157.6:c.685T>A MANE Select | NP_005148.2:p.Ser229Thr | |
| NM_007313.3:c.742T>A | NP_009297.2:p.Ser248Thr |