Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80274536G>T , CM000672.2:g.80274536G>T | GRCh38 |
| NC_000010.10:g.82034292G>T , CM000672.1:g.82034292G>T | GRCh37 |
| NC_000010.9:g.82024272G>T | NCBI36 |
| NG_008083.1:g.20143C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372213.8:c.1069C>A MANE Select | ENSP00000361287.3:p.Pro357Thr | |
| ENST00000372213.7:c.1069C>A | ENSP00000361287.3:p.Pro357Thr | |
| ENST00000480845.1:n.301C>A | ||
| ENST00000485270.5:n.581C>A | ||
| NM_000429.2:c.1069C>A | NP_000420.1:p.Pro357Thr | |
| XM_005269842.3:c.1069C>A | XP_005269899.1:p.Pro357Thr | |
| XM_005269843.3:c.946C>A | XP_005269900.1:p.Pro316Thr | |
| NM_000429.3:c.1069C>A MANE Select | NP_000420.1:p.Pro357Thr |