Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.30308352T>A , CM000685.2:g.30308352T>A | GRCh38 |
| NC_000023.10:g.30326469T>A , CM000685.1:g.30326469T>A | GRCh37 |
| NC_000023.9:g.30236390T>A | NCBI36 |
| NG_009814.1:g.6027A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378970.5:c.1012A>T MANE Select | ENSP00000368253.4:p.Thr338Ser | |
| ENST00000378963.1:c.127A>T | ENSP00000368246.1:p.Thr43Ser | |
| ENST00000378970.4:c.1012A>T | ENSP00000368253.4:p.Thr338Ser | |
| NM_000475.4:c.1012A>T | NP_000466.2:p.Thr338Ser | |
| NM_000475.5:c.1012A>T MANE Select | NP_000466.2:p.Thr338Ser |