Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133255722T= , CM000671.2:g.133255722T= | GRCh38 |
| NC_000009.11:g.136131109T= , CM000671.1:g.136131109T= | GRCh37 |
| NC_000009.10:g.135120930T= | NCBI36 |
| NG_006669.1:g.21946A= | |
| NG_006669.2:g.24494A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.1038A= | ||
| ENST00000647353.1:n.54-4570A= | ||
| ENST00000679909.1:c.28+19440A= | ENSP00000506089.1:n.28+19440A= | |
| ENST00000453660.3:n.1020A= | ||
| ENST00000538324.2:c.1006A= | ENSP00000483018.1:p.Arg336= | |
| ENST00000611156.4:c.1006A= | ENSP00000483265.1:p.Arg336= | |
| NM_020469.2:c.1009A= | NP_065202.2:p.Arg337= | |
| NM_020469.3:c.1009A= | NP_065202.2:p.Arg337= |