Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32475118G= , CM000684.2:g.32475118G= | GRCh38 |
| NC_000022.10:g.32871105G= , CM000684.1:g.32871105G= | GRCh37 |
| NC_000022.9:g.31201105G= | NCBI36 |
| NG_016001.1:g.5399G= | |
| NG_016001.2:g.5399G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266087.12:c.116G= MANE Select | ENSP00000266087.7:p.Gly39= | |
| ENST00000266087.11:c.116G= | ENSP00000266087.7:p.Gly39= | |
| ENST00000420700.5:c.116G= | ENSP00000406155.1:p.Gly39= | |
| ENST00000425028.5:c.116G= | ENSP00000395823.1:p.Gly39= | |
| ENST00000492535.1:n.104G= | ||
| NM_012179.3:c.116G= | NP_036311.3:p.Gly39= | |
| XM_011530106.1:c.-58G= | XP_011528408.1:n.-58G= | |
| XM_024452207.1:c.-75G= | XP_024307975.1:n.-75G= | |
| NM_012179.4:c.116G= MANE Select | NP_036311.3:p.Gly39= |