Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.33027730G>T , CM000683.2:g.33027730G>T | GRCh38 |
| NC_000021.8:g.34400038G>T , CM000683.1:g.34400038G>T | GRCh37 |
| NC_000021.7:g.33321908G>T | NCBI36 |
| NG_011834.1:g.6800G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382357.4:c.868G>T MANE Select | ENSP00000371794.3:p.Gly290Cys | |
| ENST00000333337.3:c.868G>T | ENSP00000331040.3:p.Gly290Cys | |
| ENST00000382357.3:c.868G>T | ENSP00000371794.3:p.Gly290Cys | |
| NM_005806.3:c.868G>T | NP_005797.1:p.Gly290Cys | |
| XM_005260908.1:c.868G>T | XP_005260965.1:p.Gly290Cys | |
| NM_005806.4:c.868G>T MANE Select | NP_005797.1:p.Gly290Cys |