Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.130383438C>T , CM000669.2:g.130383438C>T | GRCh38 |
| NC_000007.13:g.130023279C>T , CM000669.1:g.130023279C>T | GRCh37 |
| NC_000007.12:g.129810515C>T | NCBI36 |
| NG_042276.1:g.8068C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001868.4:c.531C>T MANE Select | NP_001859.1:p.Gly177= |
| ENST00000011292.8:c.531C>T MANE Select | ENSP00000011292.3:p.Gly177= |
| NM_001868.3:c.531C>T | NP_001859.1:p.Gly177= |
| ENST00000011292.7:c.531C>T | ENSP00000011292.3:p.Gly177= |
| ENST00000476062.5:c.267C>T | ENSP00000419408.1:p.Gly89= |
| ENST00000481342.5:c.267C>T | ENSP00000420218.1:p.Gly89= |
| ENST00000484324.1:c.267C>T | ENSP00000419497.1:p.Gly89= |
| ENST00000491460.5:n.493C>T | |
| ENST00000604896.5:c.142-246C>T | ENSP00000475021.1:n.142-246C>T |