Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.27865398C>G , CM000668.2:g.27865398C>G | GRCh38 |
| NC_000006.11:g.27833176C>G , CM000668.1:g.27833176C>G | GRCh37 |
| NC_000006.10:g.27941155C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003511.3:c.44C>G (H2AC16) MANE Select | NP_003502.1:p.Ala15Gly |
| ENST00000613174.2:c.44C>G (H2AC16) MANE Select | ENSP00000482538.2:p.Ala15Gly |
| NM_003511.2:c.44C>G (H2AC16) | NP_003502.1:p.Ala15Gly |
| ENST00000396980.4:c.378-346C>G (H2BC15) | ENSP00000380177.3:n.378-346C>G |
| ENST00000613174.1:c.44C>G (H2AC16) | ENSP00000482538.1:p.Ala15Gly |