Linked Data
dbSNP Id:
rs2128838549
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19956010T>A , CM000670.2:g.19956010T>A | GRCh38 |
| NC_000008.10:g.19813521T>A , CM000670.1:g.19813521T>A | GRCh37 |
| NC_000008.9:g.19857801T>A | NCBI36 |
| NG_008855.1:g.21940T>A | |
| NG_008855.2:g.59294T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000650287.1:c.945T>A MANE Select | ENSP00000497642.1:p.Tyr315Ter | |
| ENST00000650478.1:c.6T>A | ENSP00000497560.1:p.Tyr2Ter | |
| ENST00000311322.8:c.945T>A | ENSP00000309757.6:p.Tyr315Ter | |
| NM_000237.2:c.945T>A | NP_000228.1:p.Tyr315Ter | |
| NM_000237.3:c.945T>A MANE Select | NP_000228.1:p.Tyr315Ter |