Linked Data
dbSNP Id:
rs10951154
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.27095695C>A , CM000669.2:g.27095695C>A | GRCh38 |
| NC_000007.13:g.27135314C>A , CM000669.1:g.27135314C>A | GRCh37 |
| NC_000007.12:g.27101839C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000643460.2:c.218G>T MANE Select | ENSP00000494260.2:p.Arg73Leu | |
| ENST00000343060.4:c.218G>T | ENSP00000343246.4:p.Arg73Leu | |
| ENST00000355633.5:c.218G>T | ENSP00000347851.5:p.Arg73Leu | |
| NM_005522.5:c.218G>T MANE Select | NP_005513.2:p.Arg73Leu | |
| NM_153620.3:c.218G>T | NP_705873.3:p.Arg73Leu |