Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.114044289C>A , CM000672.2:g.114044289C>A | GRCh38 |
| NC_000010.10:g.115804048C>A , CM000672.1:g.115804048C>A | GRCh37 |
| NC_000010.9:g.115794038C>A | NCBI36 |
| NG_012187.1:g.5243C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000684.3:c.157C>A MANE Select | NP_000675.1:p.Leu53Met |
| ENST00000369295.4:c.157C>A MANE Select | ENSP00000358301.2:p.Leu53Met |
| NM_000684.2:c.157C>A | NP_000675.1:p.Leu53Met |
| ENST00000369295.3:c.157C>A | ENSP00000358301.2:p.Leu53Met |