Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.31580823G= , CM000664.2:g.31580823G= | GRCh38 |
| NG_008365.1:g.5149C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000348.4:c.78C= MANE Select | NP_000339.2:p.Tyr26= |
| ENST00000622030.2:c.78C= MANE Select | ENSP00000477587.1:p.Tyr26= |
| NM_000348.3:c.78C= | NP_000339.2:p.Tyr26= |
| ENST00000622030.1:c.78C= | ENSP00000477587.1:p.Tyr26= |
| XM_011533068.1:c.78C= | XP_011531370.1:p.Tyr26= |
| XM_011533070.1:c.27-47057C= | XP_011531372.1:n.27-47057C= |
| XM_011533071.1:c.27-47057C= | XP_011531373.1:n.27-47057C= |
| XM_011533072.1:c.27-47057C= | XP_011531374.1:n.27-47057C= |
| XM_011533072.2:c.27-47057C= | XP_011531374.1:n.27-47057C= |