Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154957122T= , CM000685.2:g.154957122T= | GRCh38 |
| NC_000023.10:g.154185397T= , CM000685.1:g.154185397T= | GRCh37 |
| NC_000023.9:g.153838591T= | NCBI36 |
| NG_011403.1:g.70602A= | |
| NG_011403.2:g.70602A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.1587A= MANE Select | ENSP00000353393.4:p.Lys529= | |
| ENST00000647125.1:c.*1463A= | ENSP00000496062.1:n.*1463A= | |
| ENST00000360256.8:c.1587A= | ENSP00000353393.4:p.Lys529= | |
| NM_000132.3:c.1587A= | NP_000123.1:p.Lys529= | |
| XM_011531126.1:c.1482A= | XP_011529428.1:p.Lys494= | |
| NM_000132.4:c.1587A= MANE Select | NP_000123.1:p.Lys529= |