Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133255857G= , CM000671.2:g.133255857G= | GRCh38 |
| NC_000009.11:g.136131244G= , CM000671.1:g.136131244G= | GRCh37 |
| NC_000009.10:g.135121065G= | NCBI36 |
| NG_006669.1:g.21811C= | |
| NG_006669.2:g.24359C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.903C= | ||
| ENST00000647353.1:n.54-4705C= | ||
| ENST00000679909.1:c.28+19305C= | ENSP00000506089.1:n.28+19305C= | |
| ENST00000453660.3:n.885C= | ||
| ENST00000538324.2:c.871C= | ENSP00000483018.1:p.Gln291= | |
| ENST00000611156.4:c.871C= | ENSP00000483265.1:p.Gln291= | |
| NM_020469.2:c.874C= | NP_065202.2:p.Gln292= | |
| NM_020469.3:c.874C= | NP_065202.2:p.Gln292= |