Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47373545A>C , CM000664.2:g.47373545A>C | GRCh38 |
| NC_000002.11:g.47600684A>C , CM000664.1:g.47600684A>C | GRCh37 |
| NC_000002.10:g.47454188A>C | NCBI36 |
| NG_012352.2:g.33383A>C , LRG_215:g.33383A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263735.9:c.159A>C MANE Select | ENSP00000263735.4:p.Ala53= | |
| ENST00000263735.8:c.159A>C | ENSP00000263735.4:p.Ala53= | |
| ENST00000405271.5:c.243A>C | ENSP00000385476.1:p.Ala81= | |
| ENST00000419334.1:c.387A>C | ENSP00000389028.1:p.Ala129= | |
| ENST00000456133.5:c.243A>C | ENSP00000410675.1:p.Ala81= | |
| ENST00000474691.1:n.190A>C | ||
| NM_002354.2:c.159A>C , LRG_215t1:c.159A>C | NP_002345.2:p.Ala53= | |
| NM_002354.3:c.159A>C MANE Select | NP_002345.2:p.Ala53= |