Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.27750788A>T , CM000684.2:g.27750788A>T | GRCh38 |
| NC_000022.10:g.28146776A>T , CM000684.1:g.28146776A>T | GRCh37 |
| NC_000022.9:g.26476776A>T | NCBI36 |
| NG_023258.1:g.55711T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703102.1:n.615T>A | ||
| ENST00000302326.5:c.*127T>A MANE Select | ENSP00000304956.4:n.*127T>A | |
| ENST00000302326.4:c.*127T>A | ENSP00000304956.4:n.*127T>A | |
| ENST00000424656.1:c.443T>A | ||
| ENST00000497225.1:n.446T>A | ||
| NM_002430.2:c.*127T>A | NP_002421.3:n.*127T>A | |
| NM_002430.3:c.*127T>A MANE Select | NP_002421.3:n.*127T>A |