Linked Data
MyVariant Identifiers:
chr9:g.104187811G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101425529G>T , CM000671.2:g.101425529G>T | GRCh38 |
| NC_000009.11:g.104187811G>T , CM000671.1:g.104187811G>T | GRCh37 |
| NC_000009.10:g.103227632G>T | NCBI36 |
| NG_012387.1:g.15252C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647789.2:c.723C>A MANE Select | ENSP00000497767.1:p.Thr241= | |
| ENST00000648064.1:c.723C>A | ENSP00000497990.1:p.Thr241= | |
| ENST00000648758.1:c.723C>A | ENSP00000497731.1:p.Thr241= | |
| ENST00000649902.1:c.723C>A | ENSP00000497216.1:p.Thr241= | |
| ENST00000374855.8:c.723C>A | ENSP00000363988.4:p.Thr241= | |
| ENST00000616752.1:c.723C>A | ENSP00000481363.1:p.Thr241= | |
| NM_000035.3:c.723C>A | NP_000026.2:p.Thr241= | |
| NM_000035.4:c.723C>A MANE Select | NP_000026.2:p.Thr241= |