Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.55154767C= , CM000681.2:g.55154767C= | GRCh38 |
| NC_000019.9:g.55666135C= , CM000681.1:g.55666135C= | GRCh37 |
| NC_000019.8:g.60357947C= | NCBI36 |
| NG_007866.2:g.7966G= , LRG_432:g.7966G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344887.10:c.346G= MANE Select | ENSP00000341838.5:p.Ala116= | |
| ENST00000665070.1:c.346G= | ENSP00000499482.1:p.Ala116= | |
| ENST00000344887.9:c.346G= | ENSP00000341838.5:p.Ala116= | |
| ENST00000585806.5:n.345G= | ||
| ENST00000586669.5:n.354G= | ||
| ENST00000587176.5:n.530G= | ||
| ENST00000587871.1:c.965G= | ||
| ENST00000588882.1:c.271G= | ENSP00000466729.1:p.Ala91= | |
| ENST00000590463.1:n.518G= | ||
| NM_000363.4:c.346G= , LRG_432t1:c.346G= | NP_000354.4:p.Ala116= | |
| NM_000363.5:c.346G= MANE Select | NP_000354.4:p.Ala116= |