Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160881829A= , CM000663.2:g.160881829A= | GRCh38 |
| NC_000001.10:g.160851619A= , CM000663.1:g.160851619A= | GRCh37 |
| NC_000001.9:g.159118243A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326245.4:c.405+128T= MANE Select | ENSP00000323587.3:n.405+128T= | |
| ENST00000326245.3:c.405+128T= | ENSP00000323587.3:n.405+128T= | |
| ENST00000464077.1:n.339+128T= | ||
| NM_017625.2:c.405+128T= | NP_060095.2:n.405+128T= | |
| NM_017625.3:c.405+128T= MANE Select | NP_060095.2:n.405+128T= |