Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.17872596G= , CM000681.2:g.17872596G= | GRCh38 |
| NC_000019.9:g.17983405G= , CM000681.1:g.17983405G= | GRCh37 |
| NC_000019.8:g.17844405G= | NCBI36 |
| NG_012930.1:g.5624G= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000453.3:c.277G= MANE Select | NP_000444.1:p.Gly93= |
| ENST00000222248.4:c.277G= MANE Select | ENSP00000222248.2:p.Gly93= |
| NM_000453.2:c.277G= | NP_000444.1:p.Gly93= |
| ENST00000222248.3:c.277G= | ENSP00000222248.2:p.Gly93= |
| XM_011528192.1:c.277G= | XP_011526494.1:p.Gly93= |
| XM_011528192.2:c.277G= | XP_011526494.1:p.Gly93= |
| XM_011528193.1:c.10G= | XP_011526495.1:p.Gly4= |
| XM_011528193.3:c.10G= | XP_011526495.1:p.Gly4= |
| XM_017027158.1:c.10G= | XP_016882647.1:p.Gly4= |