Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659042T>C , CM000685.2:g.136659042T>C | GRCh38 |
| NC_000023.10:g.135741201T>C , CM000685.1:g.135741201T>C | GRCh37 |
| NC_000023.9:g.135568867T>C | NCBI36 |
| NG_007280.1:g.15866T>C , LRG_141:g.15866T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000074.3:c.413T>C MANE Select | NP_000065.1:p.Leu138Ser |
| ENST00000370629.7:c.413T>C MANE Select | ENSP00000359663.2:p.Leu138Ser |
| NM_000074.2:c.413T>C , LRG_141t1:c.413T>C | NP_000065.1:p.Leu138Ser |
| ENST00000370628.2:c.350T>C | ENSP00000359662.2:p.Leu117Ser |
| ENST00000370629.6:c.413T>C | ENSP00000359663.2:p.Leu138Ser |
| ENST00000695724.1:c.*31T>C | ENSP00000512122.1:n.*31T>C |
| ENST00000695725.1:c.160T>C | ENSP00000512123.1:p.Tyr54His |
| ENST00000695726.1:n.2381T>C | |
| ENST00000695729.1:n.3216T>C |