Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.30308558A>T , CM000685.2:g.30308558A>T | GRCh38 |
| NC_000023.10:g.30326675A>T , CM000685.1:g.30326675A>T | GRCh37 |
| NC_000023.9:g.30236596A>T | NCBI36 |
| NG_009814.1:g.5821T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000475.5:c.806T>A MANE Select | NP_000466.2:p.Val269Asp |
| ENST00000378970.5:c.806T>A MANE Select | ENSP00000368253.4:p.Val269Asp |
| NM_000475.4:c.806T>A | NP_000466.2:p.Val269Asp |
| ENST00000378970.4:c.806T>A | ENSP00000368253.4:p.Val269Asp |