Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.14871438A>C , CM000667.2:g.14871438A>C | GRCh38 |
| NC_000005.9:g.14871547A>C , CM000667.1:g.14871547A>C | GRCh37 |
| NC_000005.8:g.14924547A>C | NCBI36 |
| NG_008273.1:g.5341T>G | |
| NG_008273.2:g.5348T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_054027.6:c.10T>G MANE Select | NP_473368.1:p.Phe4Val |
| ENST00000284268.8:c.10T>G MANE Select | ENSP00000284268.6:p.Phe4Val |
| NM_054027.4:c.10T>G | NP_473368.1:p.Phe4Val |
| NM_054027.5:c.10T>G | NP_473368.1:p.Phe4Val |
| ENST00000284268.6:c.10T>G | ENSP00000284268.6:p.Phe4Val |
| ENST00000505140.1:c.10T>G | ENSP00000426332.1:p.Phe4Val |
| ENST00000513115.1:n.35T>G | |
| XM_011514067.1:c.10T>G | XP_011512369.1:p.Phe4Val |