Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12790431G>T , CM000686.2:g.12790431G>T | GRCh38 |
| NC_000024.9:g.14902364G>T , CM000686.1:g.14902364G>T | GRCh37 |
| NC_000024.8:g.13411758G>T | NCBI36 |
| NG_008311.1:g.94205G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651177.1:c.3586G>T | ENSP00000498372.1:p.Ala1196Ser | |
| ENST00000338981.7:c.3586G>T MANE Select | ENSP00000342812.3:p.Ala1196Ser | |
| ENST00000426564.6:n.3598G>T | ||
| NM_004654.3:c.3586G>T | NP_004645.2:p.Ala1196Ser | |
| XM_011531469.1:c.3586G>T | XP_011529771.1:p.Ala1196Ser | |
| XM_011531470.1:c.3352G>T | XP_011529772.1:p.Ala1118Ser | |
| XM_017030078.2:c.3601G>T | XP_016885567.1:p.Ala1201Ser | |
| NM_004654.4:c.3586G>T MANE Select | NP_004645.2:p.Ala1196Ser |