Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5603372G= , CM000669.2:g.5603372G= | GRCh38 |
| NC_000007.13:g.5643003G= , CM000669.1:g.5643003G= | GRCh37 |
| NC_000007.12:g.5609529G= | NCBI36 |
| NG_030004.1:g.15568G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382361.8:c.948G= MANE Select | ENSP00000371798.3:p.Thr316= | |
| ENST00000382361.7:c.948G= | ENSP00000371798.3:p.Thr316= | |
| ENST00000405801.2:c.114G= | ENSP00000383982.2:p.Thr38= | |
| ENST00000444748.5:c.114G= | ENSP00000404506.1:p.Thr38= | |
| ENST00000447103.5:c.114G= | ENSP00000409967.1:p.Thr38= | |
| ENST00000473330.1:n.501G= | ||
| NM_003088.3:c.948G= | NP_003079.1:p.Thr316= | |
| NM_003088.4:c.948G= MANE Select | NP_003079.1:p.Thr316= |