Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94780653G>A , CM000672.2:g.94780653G>A | GRCh38 |
| NC_000010.10:g.96540410G>A , CM000672.1:g.96540410G>A | GRCh37 |
| NC_000010.9:g.96530400G>A | NCBI36 |
| NG_008384.2:g.22948G>A | |
| NG_008384.3:g.22973G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000769.4:c.636G>A MANE Select | NP_000760.1:p.Trp212Ter |
| ENST00000371321.9:c.636G>A MANE Select | ENSP00000360372.3:p.Trp212Ter |
| NM_000769.2:c.636G>A | NP_000760.1:p.Trp212Ter |
| ENST00000371321.7:c.636G>A | ENSP00000360372.3:p.Trp212Ter |
| ENST00000464755.1:c.1399G>A | ENSP00000483243.1:n.1399G>A |
| ENST00000645461.1:n.1689G>A |