Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.26104120T= , CM000668.2:g.26104120T= | GRCh38 |
| NC_000006.11:g.26104348T= , CM000668.1:g.26104348T= | GRCh37 |
| NC_000006.10:g.26212327T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003542.4:c.173T= (H4C3) MANE Select | NP_003533.1:p.Val58= |
| ENST00000377803.4:c.173T= (H4C3) MANE Select | ENSP00000367034.3:p.Val58= |
| NM_003542.3:c.173T= (H4C3) | NP_003533.1:p.Val58= |
| ENST00000377803.3:c.173T= (H4C3) | ENSP00000367034.2:p.Val58= |
| ENST00000629531.1:c.132+19653A= (H2BC3) | ENSP00000486472.1:n.132+19653A= |
| ENST00000707188.1:c.391-13086A= (H2BC4) | ENSP00000516775.1:n.391-13086A= |