Linked Data
dbSNP Id:
rs959309748
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.5692807G>T , CM000664.2:g.5692807G>T | GRCh38 |
| NC_000002.11:g.5832939G>T , CM000664.1:g.5832939G>T | GRCh37 |
| NC_000002.10:g.5750390G>T | NCBI36 |
| NG_050751.1:g.5141G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000322002.5:c.86G>T MANE Select | ENSP00000322568.3:p.Cys29Phe | |
| ENST00000322002.4:c.86G>T | ENSP00000322568.3:p.Cys29Phe | |
| NM_003108.3:c.86G>T | NP_003099.1:p.Cys29Phe | |
| NM_003108.4:c.86G>T MANE Select | NP_003099.1:p.Cys29Phe |