Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.130880101T>C , CM000671.2:g.130880101T>C | GRCh38 |
| NC_000009.11:g.133755488T>C , CM000671.1:g.133755488T>C | GRCh37 |
| NC_000009.10:g.132745309T>C | NCBI36 |
| NG_012034.1:g.171221T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005157.6:c.1457T>C MANE Select | NP_005148.2:p.Phe486Ser |
| ENST00000318560.6:c.1457T>C MANE Select | ENSP00000323315.5:p.Phe486Ser |
| NM_005157.5:c.1457T>C | NP_005148.2:p.Phe486Ser |
| NM_007313.2:c.1514T>C | NP_009297.2:p.Phe505Ser |
| NM_007313.3:c.1514T>C | NP_009297.2:p.Phe505Ser |
| ENST00000318560.5:c.1457T>C | ENSP00000323315.5:p.Phe486Ser |
| ENST00000372348.6:c.1514T>C | ENSP00000361423.2:p.Phe505Ser |
| ENST00000372348.7:c.1514T>C | ENSP00000361423.2:p.Phe505Ser |
| ENST00000372348.9:c.1514T>C | ENSP00000361423.2:p.Phe505Ser |