Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.110150332C>A , CM000675.2:g.110150332C>A | GRCh38 |
| NC_000013.10:g.110802679C>A , CM000675.1:g.110802679C>A | GRCh37 |
| NC_000013.9:g.109600680C>A | NCBI36 |
| NG_011544.2:g.161818G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001845.6:c.*31G>T MANE Select | NP_001836.3:n.*31G>T |
| ENST00000375820.10:c.*31G>T MANE Select | ENSP00000364979.4:n.*31G>T |
| NM_001845.5:c.*31G>T | NP_001836.3:n.*31G>T |
| ENST00000375820.8:c.*31G>T | ENSP00000364979.4:n.*31G>T |
| ENST00000649720.1:n.1209G>T | |
| ENST00000650424.1:c.1191G>T | |
| XM_011521048.1:c.*31G>T | XP_011519350.1:n.*31G>T |
| XM_011521048.2:c.*31G>T | XP_011519350.1:n.*31G>T |