Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101425588C>A , CM000671.2:g.101425588C>A | GRCh38 |
| NC_000009.11:g.104187870C>A , CM000671.1:g.104187870C>A | GRCh37 |
| NC_000009.10:g.103227691C>A | NCBI36 |
| NG_012387.1:g.15193G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000035.4:c.664G>T MANE Select | NP_000026.2:p.Val222Phe |
| ENST00000647789.2:c.664G>T MANE Select | ENSP00000497767.1:p.Val222Phe |
| NM_000035.3:c.664G>T | NP_000026.2:p.Val222Phe |
| ENST00000374855.8:c.664G>T | ENSP00000363988.4:p.Val222Phe |
| ENST00000468981.3:n.191G>T | |
| ENST00000616752.1:c.664G>T | ENSP00000481363.1:p.Val222Phe |
| ENST00000648064.1:c.664G>T | ENSP00000497990.1:p.Val222Phe |
| ENST00000648758.1:c.664G>T | ENSP00000497731.1:p.Val222Phe |
| ENST00000649902.1:c.664G>T | ENSP00000497216.1:p.Val222Phe |