Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.177116G>C , CM000678.2:g.177116G>C | GRCh38 |
| NC_000016.9:g.227115G>C , CM000678.1:g.227115G>C | GRCh37 |
| NC_000016.8:g.167115G>C | NCBI36 |
| NG_000006.1:g.37979G>C | |
| NG_059186.1:g.5466G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000558.5:c.283G>C MANE Select | NP_000549.1:p.Asp95His |
| ENST00000320868.9:c.283G>C MANE Select | ENSP00000322421.5:p.Asp95His |
| NM_000558.4:c.283G>C | NP_000549.1:p.Asp95His |
| ENST00000397797.1:c.187G>C | ENSP00000380899.1:p.Asp63His |
| ENST00000472694.1:n.419G>C | |
| ENST00000487791.1:n.252G>C |