Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110812185G>A , CM000672.2:g.110812185G>A | GRCh38 |
| NC_000010.10:g.112571943G>A , CM000672.1:g.112571943G>A | GRCh37 |
| NC_000010.9:g.112561933G>A | NCBI36 |
| NG_021177.1:g.172789G>A , LRG_382:g.172789G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369519.4:c.1881-93G>A MANE Select | ENSP00000358532.3:n.1881-93G>A | |
| ENST00000369519.3:c.1881-93G>A | ENSP00000358532.3:n.1881-93G>A | |
| NM_001134363.2:c.1881-93G>A | NP_001127835.2:n.1881-93G>A | |
| XM_011539697.1:c.1497-93G>A | XP_011537999.1:n.1497-93G>A | |
| XM_017016103.2:c.1716-93G>A | XP_016871592.1:n.1716-93G>A | |
| XM_017016104.2:c.1497-93G>A | XP_016871593.1:n.1497-93G>A | |
| NM_001134363.3:c.1881-93G>A MANE Select | NP_001127835.2:n.1881-93G>A |