Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48411037C>A , CM000677.2:g.48411037C>A | GRCh38 |
| NC_000015.9:g.48703234C>A , CM000677.1:g.48703234C>A | GRCh37 |
| NC_000015.8:g.46490526C>A | NCBI36 |
| NG_008805.2:g.239752G>T , LRG_778:g.239752G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.*1377G>T | ENSP00000453958.2:n.*1377G>T | |
| ENST00000682158.1:n.1950G>T | ||
| ENST00000682170.1:n.2750G>T | ||
| ENST00000682767.1:n.1866G>T | ||
| ENST00000316623.10:c.8569G>T MANE Select | ENSP00000325527.5:p.Glu2857Ter | |
| ENST00000316623.9:c.8569G>T | ENSP00000325527.5:p.Glu2857Ter | |
| ENST00000559133.5:c.3938G>T | ||
| NM_000138.4:c.8569G>T , LRG_778t1:c.8569G>T | NP_000129.3:p.Glu2857Ter | |
| NM_000138.5:c.8569G>T MANE Select | NP_000129.3:p.Glu2857Ter |