Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.47403613T>C , CM000666.2:g.47403613T>C | GRCh38 |
| NC_000004.11:g.47405630T>C , CM000666.1:g.47405630T>C | GRCh37 |
| NC_000004.10:g.47100387T>C | NCBI36 |
| NG_051831.1:g.377336T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000812.4:c.737T>C MANE Select | NP_000803.2:p.Phe246Ser |
| ENST00000295454.8:c.737T>C MANE Select | ENSP00000295454.3:p.Phe246Ser |
| NM_000812.3:c.737T>C | NP_000803.2:p.Phe246Ser |
| ENST00000295454.7:c.737T>C | ENSP00000295454.3:p.Phe246Ser |
| XM_011513678.1:c.716T>C | XP_011511980.1:p.Phe239Ser |
| XM_017007985.1:c.86T>C | XP_016863474.1:p.Phe29Ser |
| XM_024453976.1:c.638T>C | XP_024309744.1:p.Phe213Ser |
| XM_024453977.1:c.638T>C | XP_024309745.1:p.Phe213Ser |
| XM_024453978.1:c.638T>C | XP_024309746.1:p.Phe213Ser |