Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31598580G= , CM000680.2:g.31598580G= | GRCh38 |
| NC_000018.9:g.29178543G= , CM000680.1:g.29178543G= | GRCh37 |
| NC_000018.8:g.27432541G= | NCBI36 |
| NG_009490.1:g.11814G= , LRG_416:g.11814G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000371.4:c.349G= MANE Select | NP_000362.1:p.Ala117= |
| ENST00000237014.8:c.349G= MANE Select | ENSP00000237014.4:p.Ala117= |
| NM_000371.3:c.349G= , LRG_416t1:c.349G= | NP_000362.1:p.Ala117= |
| ENST00000237014.7:c.349G= | ENSP00000237014.3:p.Ala117= |
| ENST00000610404.4:c.463G= | ENSP00000477599.1:p.Ala155= |
| ENST00000610404.5:c.253G= | ENSP00000477599.2:p.Ala85= |
| ENST00000613781.1:c.349G= | ENSP00000479174.1:p.Ala117= |
| ENST00000649620.1:c.349G= | ENSP00000497927.1:p.Ala117= |