Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.121857369C= , CM000674.2:g.121857369C= | GRCh38 |
| NC_000012.11:g.122295275C= , CM000674.1:g.122295275C= | GRCh37 |
| NC_000012.10:g.120779658C= | NCBI36 |
| NG_016461.1:g.36243G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000289004.8:c.157G= (HPD) MANE Select | ENSP00000289004.4:p.Gly53= | |
| ENST00000535114.1:n.513G= (HPD) | ||
| ENST00000542159.2:n.215G= (HPD) | ||
| ENST00000543163.5:c.40G= (HPD) | ENSP00000441677.1:p.Gly14= | |
| NM_001171993.1:c.40G= (HPD) | NP_001165464.1:p.Gly14= | |
| NM_002150.2:c.157G= (HPD) | NP_002141.1:p.Gly53= | |
| XR_002957437.1:n.324-250C= (TIALD) | ||
| NM_002150.3:c.157G= (HPD) MANE Select | NP_002141.2:p.Gly53= | |
| NM_001171993.2:c.40G= (HPD) | NP_001165464.1:p.Gly14= |