Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136659219C>T , CM000685.2:g.136659219C>T | GRCh38 |
| NC_000023.10:g.135741378C>T , CM000685.1:g.135741378C>T | GRCh37 |
| NC_000023.9:g.135569044C>T | NCBI36 |
| NG_007280.1:g.16043C>T , LRG_141:g.16043C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695724.1:c.*208C>T | ENSP00000512122.1:n.*208C>T | |
| ENST00000695725.1:c.*145C>T | ENSP00000512123.1:n.*145C>T | |
| ENST00000695726.1:n.2558C>T | ||
| ENST00000695729.1:n.3393C>T | ||
| ENST00000370629.7:c.590C>T MANE Select | ENSP00000359663.2:p.Ser197Phe | |
| ENST00000370628.2:c.527C>T | ENSP00000359662.2:p.Ser176Phe | |
| ENST00000370629.6:c.590C>T | ENSP00000359663.2:p.Ser197Phe | |
| NM_000074.2:c.590C>T , LRG_141t1:c.590C>T | NP_000065.1:p.Ser197Phe | |
| NM_000074.3:c.590C>T MANE Select | NP_000065.1:p.Ser197Phe |