Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41612309C>T , CM000679.2:g.41612309C>T | GRCh38 |
| NC_000017.10:g.39768561C>T , CM000679.1:g.39768561C>T | GRCh37 |
| NC_000017.9:g.37022087C>T | NCBI36 |
| NG_008301.1:g.5519G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005557.4:c.380G>A MANE Select | NP_005548.2:p.Arg127His |
| ENST00000301653.9:c.380G>A MANE Select | ENSP00000301653.3:p.Arg127His |
| NM_005557.3:c.380G>A | NP_005548.2:p.Arg127His |
| ENST00000301653.8:c.380G>A | ENSP00000301653.3:p.Arg127His |
| ENST00000588319.1:n.457G>A | |
| ENST00000593067.1:c.-312-23G>A | ENSP00000467124.1:n.-312-23G>A |