Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.136656382C>T , CM000685.2:g.136656382C>T | GRCh38 |
| NC_000023.10:g.135738541C>T , CM000685.1:g.135738541C>T | GRCh37 |
| NC_000023.9:g.135566207C>T | NCBI36 |
| NG_007280.1:g.13206C>T , LRG_141:g.13206C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000074.3:c.373C>T MANE Select | NP_000065.1:p.His125Tyr |
| ENST00000370629.7:c.373C>T MANE Select | ENSP00000359663.2:p.His125Tyr |
| NM_000074.2:c.373C>T , LRG_141t1:c.373C>T | NP_000065.1:p.His125Tyr |
| ENST00000370628.2:c.346+1952C>T | ENSP00000359662.2:n.346+1952C>T |
| ENST00000370629.6:c.373C>T | ENSP00000359663.2:p.His125Tyr |
| ENST00000695724.1:c.315C>T | ENSP00000512122.1:p.His105= |
| ENST00000695725.1:c.157-2657C>T | ENSP00000512123.1:n.157-2657C>T |
| ENST00000695726.1:n.2341C>T | |
| ENST00000695729.1:n.3176C>T |