Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.190388184A>T , CM000665.2:g.190388184A>T | GRCh38 |
| NC_000003.11:g.190105973A>T , CM000665.1:g.190105973A>T | GRCh37 |
| NC_000003.10:g.191588667A>T | NCBI36 |
| NG_008149.1:g.5133A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264734.3:c.-146A>T MANE Select | ENSP00000264734.3:n.-146A>T | |
| ENST00000456423.2:c.-146A>T | ENSP00000414136.2:n.-146A>T | |
| ENST00000264734.2:c.65A>T | ENSP00000264734.2:p.His22Leu | |
| ENST00000456423.1:c.65A>T | ENSP00000414136.1:p.His22Leu | |
| ENST00000468220.1:n.306+13581A>T | ||
| NM_006580.3:c.65A>T | NP_006571.1:p.His22Leu | |
| NM_001378492.1:c.-93-53A>T | NP_001365421.1:n.-93-53A>T | |
| NM_001378493.1:c.-93-53A>T | NP_001365422.1:n.-93-53A>T | |
| NM_006580.4:c.-146A>T MANE Select | NP_006571.2:n.-146A>T |