Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.39581147G= , CM000677.2:g.39581147G= | GRCh38 |
| NC_000015.9:g.39873348G= , CM000677.1:g.39873348G= | GRCh37 |
| NC_000015.8:g.37660640G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260356.6:c.-111G= MANE Select | ENSP00000260356.5:n.-111G= | |
| ENST00000260356.5:c.-111G= | ENSP00000260356.5:n.-111G= | |
| ENST00000397591.2:c.-232G= | ENSP00000380720.2:n.-232G= | |
| NM_003246.2:c.-111G= | NP_003237.2:n.-111G= | |
| NM_003246.3:c.-111G= | NP_003237.2:n.-111G= | |
| XM_011521970.1:c.-232G= | XP_011520272.1:n.-232G= | |
| XM_011521971.1:c.-111G= | XP_011520273.1:n.-111G= | |
| XR_931897.1:n.65G= | ||
| XM_011521971.2:c.-111G= | XP_011520273.1:n.-111G= | |
| NM_003246.4:c.-111G= MANE Select | NP_003237.2:n.-111G= |