Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.41703696T= , CM000669.2:g.41703696T= | GRCh38 |
| NC_000007.13:g.41743294T= , CM000669.1:g.41743294T= | GRCh37 |
| NC_000007.12:g.41709819T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_027118.1:n.174-6902T= (INHBA-AS1) | |
| NR_027118.2:n.171-6902T= (INHBA-AS1) | |
| NR_027119.1:n.142-6902T= (INHBA-AS1) | |
| NR_027119.2:n.171-6902T= (INHBA-AS1) | |
| ENST00000416150.1:n.52+1588A= | |
| ENST00000638023.1:c.-225-610A= (INHBA) | ENSP00000490646.1:n.-225-610A= |
| XM_017012174.1:c.223+1588A= (INHBA) | XP_016867663.1:n.223+1588A= |
| XM_017012175.1:c.29-3179A= (INHBA) | XP_016867664.1:n.29-3179A= |
| XM_017012176.1:c.-144+1033A= (INHBA) | XP_016867665.1:n.-144+1033A= |