Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.42722238T= , CM000668.2:g.42722238T= | GRCh38 |
| NC_000006.11:g.42689976T= , CM000668.1:g.42689976T= | GRCh37 |
| NC_000006.10:g.42797954T= | NCBI36 |
| NG_009176.1:g.5383A= | |
| NG_009176.2:g.5383A= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000230381.7:c.97A= MANE Select | ENSP00000230381.5:p.Ile33= | |
| ENST00000230381.6:c.97A= | ENSP00000230381.5:p.Ile33= | |
| NM_000322.4:c.97A= | NP_000313.2:p.Ile33= | |
| XR_427834.2:n.752A= | ||
| XR_926295.1:n.752A= | ||
| XR_427834.4:n.802A= | ||
| XR_926295.3:n.802A= | ||
| NM_000322.5:c.97A= MANE Select | NP_000313.2:p.Ile33= |