Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154961120C>A , CM000685.2:g.154961120C>A | GRCh38 |
| NC_000023.10:g.154189395C>A , CM000685.1:g.154189395C>A | GRCh37 |
| NC_000023.9:g.153842589C>A | NCBI36 |
| NG_011403.1:g.66604G>T | |
| NG_011403.2:g.66604G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.1492G>T MANE Select | NP_000123.1:p.Gly498Ter |
| ENST00000360256.9:c.1492G>T MANE Select | ENSP00000353393.4:p.Gly498Ter |
| NM_000132.3:c.1492G>T | NP_000123.1:p.Gly498Ter |
| ENST00000360256.8:c.1492G>T | ENSP00000353393.4:p.Gly498Ter |
| ENST00000647125.1:c.*1368G>T | ENSP00000496062.1:n.*1368G>T |
| XM_011531126.1:c.1387G>T | XP_011529428.1:p.Gly463Ter |