Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.96265237C= , CM000664.2:g.96265237C= | GRCh38 |
| NC_000002.11:g.96930975C= , CM000664.1:g.96930975C= | GRCh37 |
| NC_000002.10:g.96294702C= | NCBI36 |
| NG_027695.1:g.5777G= , LRG_528:g.5777G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000258439.8:c.145G= MANE Select | ENSP00000258439.3:p.Ala49= | |
| ENST00000258439.7:c.145G= | ENSP00000258439.2:p.Ala49= | |
| ENST00000432959.1:c.145G= | ENSP00000416660.1:p.Ala49= | |
| NM_001193304.2:c.145G= | NP_001180233.1:p.Ala49= | |
| NM_017849.3:c.145G= , LRG_528t1:c.145G= | NP_060319.1:p.Ala49= | |
| NM_001193304.3:c.145G= | NP_001180233.1:p.Ala49= | |
| NM_017849.4:c.145G= MANE Select | NP_060319.1:p.Ala49= |