Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.48703065G= , CM000681.2:g.48703065G= | GRCh38 |
| NC_000019.9:g.49206322G= , CM000681.1:g.49206322G= | GRCh37 |
| NC_000019.8:g.53898134G= | NCBI36 |
| NG_007511.1:g.12095G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000425340.3:c.109G= MANE Select | ENSP00000387498.2:p.Ala37= | |
| ENST00000522966.2:c.109G= | ENSP00000430227.2:p.Ala37= | |
| ENST00000391876.5:c.109G= | ENSP00000375748.4:p.Ala37= | |
| ENST00000425340.2:c.109G= | ENSP00000387498.2:p.Ala37= | |
| ENST00000522966.1:c.109G= | ENSP00000430227.1:p.Ala37= | |
| NM_000511.5:c.109G= | NP_000502.4:p.Ala37= | |
| NM_001097638.2:c.109G= | NP_001091107.1:p.Ala37= | |
| NR_131188.1:n.784C= | ||
| NM_000511.6:c.109G= MANE Select | NP_000502.4:p.Ala37= | |
| NM_001097638.3:c.109G= | NP_001091107.1:p.Ala37= |