Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.186539530A>T , CM000665.2:g.186539530A>T | GRCh38 |
| NC_000003.11:g.186257319A>T , CM000665.1:g.186257319A>T | GRCh37 |
| NC_000003.10:g.187740013A>T | NCBI36 |
| NG_009829.1:g.9849T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307944.6:c.89T>A MANE Select | ENSP00000312099.5:p.Phe30Tyr | |
| ENST00000307944.5:c.89T>A | ENSP00000312099.5:p.Phe30Tyr | |
| ENST00000392499.6:c.89T>A | ENSP00000376287.2:p.Phe30Tyr | |
| ENST00000460288.1:n.991T>A | ||
| NM_017541.2:c.89T>A | NP_060011.1:p.Phe30Tyr | |
| NM_017541.3:c.89T>A | NP_060011.1:p.Phe30Tyr | |
| NM_017541.4:c.89T>A MANE Select | NP_060011.1:p.Phe30Tyr |