Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45500413G= , CM000663.2:g.45500413G= | GRCh38 |
| NC_000001.10:g.45966085G= , CM000663.1:g.45966085G= | GRCh37 |
| NC_000001.9:g.45738672G= | NCBI36 |
| NG_013378.1:g.5230G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000401061.9:c.81G= MANE Select | ENSP00000383840.4:p.Gln27= | |
| ENST00000401061.8:c.81G= | ENSP00000383840.4:p.Gln27= | |
| ENST00000616135.1:c.-91G= | ENSP00000478859.1:n.-91G= | |
| NM_015506.2:c.81G= | NP_056321.2:p.Gln27= | |
| XM_005270724.3:c.81G= | XP_005270781.1:p.Gln27= | |
| XM_011541204.1:c.-142G= | XP_011539506.1:n.-142G= | |
| NM_001330540.1:c.-142G= | NP_001317469.1:n.-142G= | |
| XM_005270724.5:c.81G= | XP_005270781.1:p.Gln27= | |
| NM_015506.3:c.81G= MANE Select | NP_056321.2:p.Gln27= | |
| NM_001330540.2:c.-142G= | NP_001317469.1:n.-142G= |