Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42721642C= , CM000668.2:g.42721642C= | GRCh38 |
| NC_000006.11:g.42689380C= , CM000668.1:g.42689380C= | GRCh37 |
| NC_000006.10:g.42797358C= | NCBI36 |
| NG_009176.1:g.5979G= | |
| NG_009176.2:g.5979G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230381.7:c.581+112G= MANE Select | ENSP00000230381.5:n.581+112G= | |
| ENST00000230381.6:c.581+112G= | ENSP00000230381.5:n.581+112G= | |
| NM_000322.4:c.581+112G= | NP_000313.2:n.581+112G= | |
| XR_427834.2:n.1236+112G= | ||
| XR_926295.1:n.1236+112G= | ||
| XR_427834.4:n.1286+112G= | ||
| XR_926295.3:n.1286+112G= | ||
| NM_000322.5:c.581+112G= MANE Select | NP_000313.2:n.581+112G= |