Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80280273A>T , CM000672.2:g.80280273A>T | GRCh38 |
| NC_000010.10:g.82040029A>T , CM000672.1:g.82040029A>T | GRCh37 |
| NC_000010.9:g.82030009A>T | NCBI36 |
| NG_008083.1:g.14406T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372213.8:c.449T>A MANE Select | ENSP00000361287.3:p.Met150Lys | |
| ENST00000372213.7:c.449T>A | ENSP00000361287.3:p.Met150Lys | |
| ENST00000455001.1:c.260T>A | ENSP00000414961.1:p.Met87Lys | |
| NM_000429.2:c.449T>A | NP_000420.1:p.Met150Lys | |
| XM_005269842.3:c.449T>A | XP_005269899.1:p.Met150Lys | |
| XM_005269843.3:c.326T>A | XP_005269900.1:p.Met109Lys | |
| NM_000429.3:c.449T>A MANE Select | NP_000420.1:p.Met150Lys |