Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.94769136C>T , CM000676.2:g.94769136C>T | GRCh38 |
| NC_000014.8:g.95235473C>T , CM000676.1:g.95235473C>T | GRCh37 |
| NC_000014.7:g.94305226C>T | NCBI36 |
| NG_034111.1:g.6027G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_173849.3:c.437G>A MANE Select | NP_776248.1:p.Arg146His |
| ENST00000238558.5:c.437G>A MANE Select | ENSP00000238558.3:p.Arg146His |
| NM_173849.2:c.437G>A | NP_776248.1:p.Arg146His |
| ENST00000238558.4:c.437G>A | ENSP00000238558.3:p.Arg146His |