Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.49016181C>T , CM000681.2:g.49016181C>T | GRCh38 |
| NC_000019.9:g.49519438C>T , CM000681.1:g.49519438C>T | GRCh37 |
| NC_000019.8:g.54211250C>T | NCBI36 |
| NG_011464.1:g.5910G>A | |
| NG_033041.1:g.27283C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649238.3:c.313G>A MANE Select | ENSP00000497294.2:p.Ala105Thr | |
| ENST00000649284.1:n.404G>A | ||
| ENST00000221421.6:c.313G>A | ENSP00000221421.1:p.Ala105Thr | |
| ENST00000391869.4:c.307G>A | ENSP00000375742.4:p.Ala103Thr | |
| NM_000894.2:c.313G>A | NP_000885.1:p.Ala105Thr | |
| XM_011526975.1:c.361G>A | XP_011525277.1:p.Ala121Thr | |
| NM_000894.3:c.313G>A MANE Select | NP_000885.1:p.Ala105Thr |