Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.56594529G= , CM000679.2:g.56594529G= | GRCh38 |
| NC_000017.10:g.54671890G= , CM000679.1:g.54671890G= | GRCh37 |
| NC_000017.9:g.52026889G= | NCBI36 |
| NG_011958.1:g.5831G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000332822.6:c.306G= MANE Select | ENSP00000328181.4:p.Ala102= | |
| ENST00000332822.4:c.306G= | ENSP00000328181.4:p.Ala102= | |
| NM_005450.4:c.306G= | NP_005441.1:p.Ala102= | |
| NM_005450.6:c.306G= MANE Select | NP_005441.1:p.Ala102= |