Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133256068G= , CM000671.2:g.133256068G= | GRCh38 |
| NC_000009.11:g.136131455G= , CM000671.1:g.136131455G= | GRCh37 |
| NC_000009.10:g.135121276G= | NCBI36 |
| NG_006669.1:g.21600C= | |
| NG_006669.2:g.24148C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.692C= | ||
| ENST00000647353.1:n.54-4916C= | ||
| ENST00000679909.1:c.28+19094C= | ENSP00000506089.1:n.28+19094C= | |
| ENST00000453660.3:n.674C= | ||
| ENST00000538324.2:c.660C= | ENSP00000483018.1:p.Gly220= | |
| ENST00000611156.4:c.660C= | ENSP00000483265.1:p.Gly220= | |
| NM_020469.2:c.663C= | NP_065202.2:p.Gly221= | |
| NM_020469.3:c.663C= | NP_065202.2:p.Gly221= |