Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.38880390T>C , CM000675.2:g.38880390T>C | GRCh38 |
| NC_000013.10:g.39454527T>C , CM000675.1:g.39454527T>C | GRCh37 |
| NC_000013.9:g.38352527T>C | NCBI36 |
| NG_008125.2:g.198355T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_207361.6:c.9113T>C MANE Select | NP_997244.4:p.Val3038Ala |
| ENST00000280481.9:c.9113T>C MANE Select | ENSP00000280481.7:p.Val3038Ala |
| NM_207361.5:c.9113T>C | NP_997244.4:p.Val3038Ala |
| ENST00000280481.8:c.9113T>C | ENSP00000280481.7:p.Val3038Ala |