Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.21481557T= , CM000671.2:g.21481557T= | GRCh38 |
| NC_000009.11:g.21481556T= , CM000671.1:g.21481556T= | GRCh37 |
| NC_000009.10:g.21471556T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_176891.5:c.138A= (IFNE) MANE Select | NP_795372.1:p.Gln46= |
| ENST00000448696.4:c.138A= (IFNE) MANE Select | ENSP00000418018.2:p.Gln46= |
| NM_176891.4:c.138A= (IFNE) | NP_795372.1:p.Gln46= |
| NR_027054.1:n.211-4265A= (MIR31HG) | |
| NR_027054.2:n.311-4265A= (MIR31HG) | |
| NR_152877.1:n.52-4265A= (MIR31HG) | |
| NR_152878.1:n.52-4265A= (MIR31HG) | |
| NR_152879.1:n.311-4265A= (MIR31HG) |