Linked Data
dbSNP Id:
rs145657341
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19951811G>T , CM000670.2:g.19951811G>T | GRCh38 |
| NC_000008.10:g.19809322G>T , CM000670.1:g.19809322G>T | GRCh37 |
| NC_000008.9:g.19853602G>T | NCBI36 |
| NG_008855.1:g.17741G>T | |
| NG_008855.2:g.55095G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.292G>T MANE Select | ENSP00000497642.1:p.Ala98Ser | |
| ENST00000311322.8:c.292G>T | ENSP00000309757.6:p.Ala98Ser | |
| ENST00000520959.5:c.64G>T | ENSP00000428496.1:p.Ala22Ser | |
| ENST00000521994.1:n.549G>T | ||
| ENST00000522701.5:c.292G>T | ENSP00000428557.1:p.Ala98Ser | |
| ENST00000524029.5:c.292G>T | ENSP00000428237.1:p.Ala98Ser | |
| NM_000237.2:c.292G>T | NP_000228.1:p.Ala98Ser | |
| NM_000237.3:c.292G>T MANE Select | NP_000228.1:p.Ala98Ser |