Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110601966T>G , CM000672.2:g.110601966T>G | GRCh38 |
| NC_000010.10:g.112361724T>G , CM000672.1:g.112361724T>G | GRCh37 |
| NC_000010.9:g.112351714T>G | NCBI36 |
| NG_012217.1:g.39276T>G , LRG_774:g.39276T>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005445.4:c.2893T>G MANE Select | NP_005436.1:p.Leu965Val |
| ENST00000361804.5:c.2893T>G MANE Select | ENSP00000354720.5:p.Leu965Val |
| NM_005445.3:c.2893T>G , LRG_774t1:c.2893T>G | NP_005436.1:p.Leu965Val |
| ENST00000361804.4:c.2893T>G | ENSP00000354720.4:p.Leu965Val |
| ENST00000684988.1:n.5126T>G | |
| ENST00000685743.1:n.2601T>G | |
| ENST00000686057.1:n.1244T>G | |
| ENST00000689321.1:n.1856T>G | |
| ENST00000689986.1:n.682T>G |