Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.60648804T>G , CM000676.2:g.60648804T>G | GRCh38 |
| NC_000014.8:g.61115522T>G , CM000676.1:g.61115522T>G | GRCh37 |
| NC_000014.7:g.60185275T>G | NCBI36 |
| NG_008231.1:g.5634A>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005982.4:c.386A>C MANE Select | NP_005973.1:p.Tyr129Ser |
| ENST00000645694.3:c.386A>C MANE Select | ENSP00000494686.1:p.Tyr129Ser |
| NM_005982.3:c.386A>C | NP_005973.1:p.Tyr129Ser |
| ENST00000247182.6:c.386A>C | ENSP00000247182.5:p.Tyr129Ser |
| ENST00000553535.2:n.249-2227A>C | |
| ENST00000554986.2:c.42-2227A>C | ENSP00000452700.2:n.42-2227A>C |
| ENST00000555955.3:n.1198-2227A>C | |
| XM_017021602.2:c.386A>C | XP_016877091.1:p.Tyr129Ser |