Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133255707T= , CM000671.2:g.133255707T= | GRCh38 |
| NC_000009.11:g.136131094T= , CM000671.1:g.136131094T= | GRCh37 |
| NC_000009.10:g.135120915T= | NCBI36 |
| NG_006669.1:g.21961A= | |
| NG_006669.2:g.24509A= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000453660.4:n.1053A= | ||
| ENST00000647353.1:n.54-4555A= | ||
| ENST00000679909.1:c.28+19455A= | ENSP00000506089.1:n.28+19455A= | |
| ENST00000453660.3:n.1035A= | ||
| ENST00000538324.2:c.1021A= | ENSP00000483018.1:p.Thr341= | |
| ENST00000611156.4:c.1021A= | ENSP00000483265.1:p.Thr341= | |
| NM_020469.2:c.1024A= | NP_065202.2:p.Thr342= | |
| NM_020469.3:c.1024A= | NP_065202.2:p.Thr342= |