Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.64162893C>A , CM000677.2:g.64162893C>A | GRCh38 |
| NC_000015.9:g.64455092C>A , CM000677.1:g.64455092C>A | GRCh37 |
| NC_000015.8:g.62242145C>A | NCBI36 |
| NG_012979.1:g.5263G>T , LRG_10:g.5263G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300026.4:c.94G>T MANE Select | ENSP00000300026.4:p.Ala32Ser | |
| ENST00000561048.2:n.127G>T | ||
| ENST00000680158.1:c.94G>T | ENSP00000504873.1:p.Ala32Ser | |
| ENST00000681397.1:c.94G>T | ENSP00000506584.1:p.Ala32Ser | |
| ENST00000681658.1:c.30+64G>T | ENSP00000505431.1:n.30+64G>T | |
| ENST00000300026.3:c.94G>T | ENSP00000300026.3:p.Ala32Ser | |
| ENST00000558492.1:n.114G>T | ||
| ENST00000561048.1:n.129G>T | ||
| NM_000942.4:c.94G>T , LRG_10t1:c.94G>T | NP_000933.1:p.Ala32Ser | |
| NM_000942.5:c.94G>T MANE Select | NP_000933.1:p.Ala32Ser |