Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.13884763G>A , CM000680.2:g.13884763G>A | GRCh38 |
| NC_000018.9:g.13884762G>A , CM000680.1:g.13884762G>A | GRCh37 |
| NC_000018.8:g.13874762G>A | NCBI36 |
| NG_011819.1:g.35774C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000529.2:c.756C>T MANE Select | NP_000520.1:p.Ala252= |
| ENST00000327606.4:c.756C>T MANE Select | ENSP00000333821.2:p.Ala252= |
| NM_001291911.1:c.756C>T | NP_001278840.1:p.Ala252= |
| ENST00000327606.3:c.756C>T | ENSP00000333821.2:p.Ala252= |
| XM_017025781.1:c.756C>T | XP_016881270.1:p.Ala252= |