Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7525075T>A , CM000681.2:g.7525075T>A | GRCh38 |
| NC_000019.9:g.7589961T>A , CM000681.1:g.7589961T>A | GRCh37 |
| NC_000019.8:g.7495961T>A | NCBI36 |
| NG_015806.1:g.7466T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.146T>A MANE Select | ENSP00000264079.5:p.Phe49Tyr | |
| ENST00000264079.10:c.146T>A | ENSP00000264079.5:p.Phe49Tyr | |
| ENST00000394321.9:n.226T>A | ||
| ENST00000596390.1:n.262T>A | ||
| ENST00000601003.1:c.146T>A | ENSP00000469074.1:p.Phe49Tyr | |
| NM_020533.2:c.146T>A | NP_065394.1:p.Phe49Tyr | |
| NM_020533.3:c.146T>A MANE Select | NP_065394.1:p.Phe49Tyr |