Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.27750777T>A , CM000684.2:g.27750777T>A | GRCh38 |
| NC_000022.10:g.28146765T>A , CM000684.1:g.28146765T>A | GRCh37 |
| NC_000022.9:g.26476765T>A | NCBI36 |
| NG_023258.1:g.55722A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703102.1:n.626A>T | ||
| ENST00000302326.5:c.*138A>T MANE Select | ENSP00000304956.4:n.*138A>T | |
| ENST00000302326.4:c.*138A>T | ENSP00000304956.4:n.*138A>T | |
| ENST00000424656.1:c.454A>T | ||
| ENST00000497225.1:n.457A>T | ||
| NM_002430.2:c.*138A>T | NP_002421.3:n.*138A>T | |
| NM_002430.3:c.*138A>T MANE Select | NP_002421.3:n.*138A>T |