Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.44823156C>T , CM000663.2:g.44823156C>T | GRCh38 |
| NC_000001.10:g.45288828C>T , CM000663.1:g.45288828C>T | GRCh37 |
| NC_000001.9:g.45061415C>T | NCBI36 |
| NG_013369.1:g.24789G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003738.5:c.3270G>A MANE Select | NP_003729.3:p.Ala1090= |
| ENST00000372192.4:c.3270G>A MANE Select | ENSP00000361266.3:p.Ala1090= |
| NM_001166292.1:c.3270G>A | NP_001159764.1:p.Ala1090= |
| NM_001166292.2:c.3270G>A | NP_001159764.1:p.Ala1090= |
| NM_003738.4:c.3270G>A | NP_003729.3:p.Ala1090= |
| ENST00000372192.3:c.3270G>A | ENSP00000361266.3:p.Ala1090= |
| ENST00000438067.5:c.31G>A | |
| ENST00000447098.6:c.3270G>A | ENSP00000389703.2:p.Ala1090= |